{"data":{"company":{"name":"IQVIA Biotech","slug":"iqvia-biotech","logo_url":"https://logos.yubhub.co/jobs.iqvia.com.png","canonical_domain":"jobs.iqvia.com","editorial":null,"wikidata_id":null,"founded":null,"ceo":null,"founders":[],"hq_location":null,"industry":null,"employee_count":null,"official_website":null,"wikipedia_url":null,"stock_ticker":null,"stock_price":null,"market_cap":null,"revenue":null,"ipo_date":null,"sector":null,"full_time_employees":null,"company_description":null,"twitter_username":null,"linkedin_id":null,"instagram_username":null,"facebook_id":null,"parent_org":null,"country":null,"github_org":null,"github_public_repos":null,"github_followers":null,"github_verified":0,"github_description":null,"github_location":null,"github_blog":null,"github_twitter":null,"stock_exchange":null,"stock_beta":null,"stock_range":null,"stock_is_actively_trading":null,"fmp_image":null,"fmp_address":null,"fmp_city":null,"fmp_state":null,"fmp_country":null,"recent_news":[],"search_interest_index":null,"search_interest_trend":null,"wikipedia_monthly_views":null,"hn_mention_count":null,"hn_top_stories":[],"wayback_first_year":null,"sec_incorporation_state":null,"sec_latest_filing_type":null,"sec_latest_filing_date":null,"sec_filings":[],"research_papers_count":null,"research_citations_count":null,"research_h_index":null,"research_topics":[],"is_federal_contractor":null,"earnings_calendar":[],"industry_canonical":null,"enrichment_sources":[],"last_enriched_at":null},"hiring":{"total_jobs":25,"categories":[{"category":"healthcare","count":24},{"category":"research","count":1}],"experience_levels":[{"level":"senior","count":24},{"level":"mid","count":1}],"work_arrangements":[{"arrangement":"remote","count":5},{"arrangement":"onsite","count":5}],"top_titles":[{"title":"Sr. Site Contracts Associate","count":5},{"title":"Senior Site Contracts Associate","count":2},{"title":"Senior Clinical Research Associate (Sr CRA 3)","count":2},{"title":"CRA 2","count":2},{"title":"CPM/Sr CPM","count":2},{"title":"Sr. CRA 1","count":1},{"title":"Sr. Clinical Project Manager","count":1},{"title":"Senior Clinical Trial Manager","count":1},{"title":"Senior Clinical Research Associate","count":1},{"title":"Senior Clinical Project Manager or Clinical Project Manager","count":1},{"title":"Oncology & Global Experience Clinical Leads","count":1},{"title":"Global Study Manager","count":1},{"title":"CTM II or Senior CTM","count":1},{"title":"Clinical Trial Manager II","count":1},{"title":"Clinical Research Associate II","count":1}],"locations":[{"location":"são paulo","count":5},{"location":"buenos aires","count":3},{"location":"warsaw","count":1},{"location":"milan","count":1},{"location":"mexico city","count":1},{"location":"kirkland, quebec","count":1},{"location":"frankfurt, hesse","count":1},{"location":"durham, north carolina","count":1},{"location":"amsterdam","count":1}],"skills":[{"skill":"Good Clinical Practice GCP","required":8,"preferred":0,"total":8},{"skill":"Project Management","required":8,"preferred":0,"total":8},{"skill":"Life Sciences","required":6,"preferred":1,"total":7},{"skill":"Gcp/ich","required":7,"preferred":0,"total":7},{"skill":"Communication","required":6,"preferred":0,"total":6},{"skill":"Microsoft Office","required":6,"preferred":0,"total":6},{"skill":"Clinical Research","required":6,"preferred":0,"total":6},{"skill":"Regulatory Requirements","required":6,"preferred":0,"total":6},{"skill":"ICH Guidelines","required":5,"preferred":0,"total":5},{"skill":"Clinical Trial Contract Management","required":4,"preferred":0,"total":4},{"skill":"FDA Regulations","required":4,"preferred":0,"total":4},{"skill":"Clinical Trial Processes","required":4,"preferred":0,"total":4},{"skill":"English","required":4,"preferred":0,"total":4},{"skill":"Regulatory Guidelines","required":4,"preferred":0,"total":4},{"skill":"Monitoring","required":3,"preferred":0,"total":3},{"skill":"Microsoft Office Applications","required":3,"preferred":0,"total":3},{"skill":"Clinical Trial Systems","required":3,"preferred":0,"total":3},{"skill":"Therapeutic Area Knowledge","required":0,"preferred":3,"total":3},{"skill":"Protocol Management","required":0,"preferred":3,"total":3},{"skill":"Clinical Trial Management","required":3,"preferred":0,"total":3}],"salary_stats":{"count":9,"min":60400,"q1":124800,"median":151300,"q3":162950,"max":311200},"job_types":[{"type":"full-time","count":24}],"latest_jobs":[{"id":"job_724c4f38-54b","title":"Clinical Research Associate II","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kirkland-Quebec-Canada/Attach-de-recherche-clinique-II--Oncologie--Clinical-Research-Associate-II--Oncology--IQVIA-Biotech_R1565812","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":"remote","category":"Research","description":"<p>IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology monitoring experience. This role is home-based in Eastern Canada and requires fluency in both French and English.</p>\n<p>The CRA II is responsible for monitoring Phase I–IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from start-up through close-out.</p>\n<p>Key Responsibilities:</p>\n<ul>\n<li>Conduct site selection, initiation, monitoring, and close-out visits</li>\n<li>Train site personnel on study protocols, EDC systems, and study requirements</li>\n<li>Ensure high-quality source documentation, data integrity, and timely query resolution</li>\n<li>Oversee IP accountability and regulatory document collection</li>\n<li>Serve as the primary site contact and maintain regular communication</li>\n<li>Prepare monitoring reports following Standard Operating Procedures and timelines</li>\n<li>Support investigator meetings and collaborate with CTMs/Lead CRAs</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bilingual in French and English (Required)</li>\n<li>Bachelor’s Degree required. Preference in life sciences or related discipline. Equivalent combination of education, training and experience may be accepted in lieu of degree.</li>\n<li>At least 1 year of onsite monitoring experience (Required)</li>\n<li>Ability to travel 65–70%</li>\n</ul>\n<p>The potential base pay range for this role, when annualized, is $74,700.00 - $124,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and wellness and/or other benefits.</p>","enriched_at":1793326544536},{"id":"job_fec13323-1dc","title":"Senior Clinical Project Manager or Clinical Project Manager","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Durham-North-Carolina-United-States-of-America/XMLNAME--Senior--Clinical-Project-Manager--IQVIA-Biotech_R1571841","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>IQVIA Biotech is seeking an experienced Senior Clinical Project Manager or Clinical Project Manager to drive the successful delivery of clinical trials. As a Senior Clinical Project Manager or Clinical Project Manager, you will lead the planning and execution of global and multi-regional clinical studies from start-up through closeout.</p>\n<p>Key Responsibilities:</p>\n<ul>\n<li>Lead the planning and execution of global and multi-regional clinical studies from start-up through closeout.</li>\n<li>Serve as the primary point of contact for sponsors and maintain strong customer relationships.</li>\n<li>Develop and implement integrated study management plans in collaboration with cross-functional teams.</li>\n<li>Drive study delivery while optimizing timelines, quality, and budget performance.</li>\n<li>Provide strategic leadership for project teams, setting objectives and ensuring accountability for key milestones.</li>\n<li>Identify, assess, and proactively manage project risks, issues, and change requests.</li>\n<li>Monitor project progress and communicate study status, metrics, and key updates to internal and external stakeholders.</li>\n<li>Ensure compliance with applicable regulations, ICH-GCP guidelines, SOPs, and study-specific requirements.</li>\n<li>Support business development activities, including proposal development and bid defense presentations.</li>\n<li>Oversee project financial performance, including forecasting, budget management, and scope change management.</li>\n<li>Mentor and support the development of project team members while fostering collaboration across functions and regions.</li>\n<li>Drive continuous improvement by sharing lessons learned and promoting best practices.</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor’s degree in Life Sciences or a related field.</li>\n<li>Minimum of 7 years of clinical research experience, including at least 4 years of clinical project management experience.</li>\n<li>Strong understanding of clinical trial conduct, ICH-GCP, regulatory requirements, and global drug development processes.</li>\n<li>Experience managing small to medium, full-service, multi-country, and/or multi-regional clinical studies.</li>\n<li>Proven ability to lead cross-functional teams and manage complex stakeholder relationships.</li>\n<li>Strong financial acumen with experience managing project budgets, forecasting, and scope changes.</li>\n<li>Excellent communication, presentation, negotiation, and problem-solving skills.</li>\n</ul>\n<p>The potential base pay range for this role, when annualized, is $68,400.00 - $232,800.00.</p>","enriched_at":1793321365136},{"id":"job_33187e43-f70","title":"Senior Clinical Research Associate","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Durham-North-Carolina-United-States-of-America/Sr-CRA--Oncology--IQVIA-Biotech_R1571573-4","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>IQVIA Biotech is seeking an experienced Senior Clinical Research Associate to join their Clinical Monitoring team.</p>\n<p>In this role, you will independently manage and monitor clinical trial sites to ensure studies are conducted in compliance with study protocols, Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, regulatory requirements, and sponsor expectations.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Performing site monitoring activities, including site qualification, initiation, routine monitoring, and closeout visits</li>\n<li>Partnering with investigative sites to support patient recruitment and retention efforts</li>\n<li>Providing protocol and study-related training</li>\n<li>Proactively identifying and resolving quality or compliance issues</li>\n<li>Overseeing site performance, tracking study milestones, reviewing source documentation, and managing data query resolution</li>\n<li>Collaborating with cross-functional teams to support the successful execution of clinical trials</li>\n<li>Mentoring junior CRAs through co-monitoring and training activities</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree in a scientific, healthcare, or related discipline</li>\n<li>Minimum of 4 years of on-site clinical monitoring experience</li>\n<li>Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical trial processes</li>\n<li>Experience conducting monitoring visits across multiple phases of clinical research</li>\n<li>Excellent organizational, communication, and problem-solving skills</li>\n<li>Ability to effectively manage multiple priorities in a fast-paced environment</li>\n<li>Proficiency with Microsoft Office applications and clinical trial systems</li>\n</ul>\n<p>Preferred skills:</p>\n<ul>\n<li>Strong therapeutic area knowledge and protocol management experience</li>\n<li>Proven ability to build productive relationships with investigative sites, sponsors, and internal study teams</li>\n<li>Experience mentoring or supporting the development of junior clinical research professionals</li>\n</ul>\n<p>The potential base pay range for this role is $105,100.00 - $197,500.00 per year.</p>","enriched_at":1793320361164},{"id":"job_f1e41530-49f","title":"Sr. Site Contracts Associate","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Frankfurt-Hesse-Germany/Senior-Site-Contracts-Associate--IQVIA-Biotech---Germany_R1566236","location":"Frankfurt, Hesse","job_type":"full-time","experience_level":"senior","work_arrangement":"remote","category":"Healthcare","description":"<p>IQVIA Biotech is seeking an experienced Senior Site Contracts Associate to manage contract strategy and oversee all start-up contracting activities for selected sponsors.</p>\n<p>In this role, you will support complex studies and multi-protocol programs, ensuring high-quality delivery and operational excellence.</p>\n<p>Key Responsibilities:</p>\n<ul>\n<li>Develop complex investigator grant estimates, contracting strategies, and proposal text to support business development.</li>\n<li>Create and maintain contract and budget templates, systems, tools, processes, and training materials for complex studies and multi-protocol programs.</li>\n<li>Collaborate closely with sponsors, stakeholders, and RSU regional teams to ensure successful delivery of the project scope and compliance with sponsor requirements.</li>\n<li>Provide legal, operational, and financial contracting expertise to support site agreements and facilitate efficient study start-up and maintenance.</li>\n<li>Create and review scientific, technical, and administrative documentation required for study initiation.</li>\n<li>Assess the contracting landscape and contribute to the analysis and dissemination of contracting intelligence across the company.</li>\n<li>Ensure contracting efficiency, adherence to timelines, and achievement of financial targets.</li>\n<li>Track and report contracting performance metrics and out-of-scope activities.</li>\n<li>Partner with Quality Management to uphold high contract management and quality standards.</li>\n<li>Mentor and coach colleagues, delivering training and technical guidance.</li>\n<li>Present to clients and professional bodies as needed.</li>\n<li>Maintain accurate internal system documentation, including CTMS, trackers, and project plans.</li>\n<li>Build and maintain strong relationships with preferred clients, serving as liaison for key accounts when required.</li>\n</ul>\n<p>Qualifications &amp; Experience:</p>\n<ul>\n<li>Bachelor’s degree in a related field (required).</li>\n<li>5+ years of site contracting experience within a sponsor or CRO, including demonstrable experience as an international contract expert.</li>\n<li>Equivalent combinations of education, training, and experience will be considered.</li>\n<li>Strong negotiation and communication skills, with the ability to challenge and influence.</li>\n<li>Excellent interpersonal skills and proven success working within matrix teams.</li>\n<li>Advanced legal, financial, and technical writing abilities.</li>\n<li>Solid understanding of clinical trial regulations, GCP/ICH, and the overall drug development process.</li>\n<li>Knowledge of local and global regulatory requirements, SOPs, and corporate standards.</li>\n<li>Ability to exercise independent judgment and take calculated risks.</li>\n<li>Strong project leadership skills and experience mentoring others.</li>\n<li>Excellent planning, organizational, and presentation skills.</li>\n<li>Strong proficiency in Microsoft Word, Excel, and other Office tools.</li>\n<li>Deep knowledge of clinical trial contract management processes.</li>\n<li>Proven experience leveraging metrics to establish timelines and deliverables.</li>\n<li>Ability to initiate and grow programs across departments to drive organizational impact.</li>\n</ul>\n<p>What We Offer:</p>\n<ul>\n<li>Opportunity to work on global, high-complexity clinical programs.</li>\n<li>A collaborative, supportive, and growth-oriented environment.</li>\n<li>The chance to influence key clients and shape contracting strategy at scale.</li>\n<li>Career progression and professional development opportunities.</li>\n</ul>","enriched_at":1793310857268},{"id":"job_d8be68b3-ed4","title":"CRA 2","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Durham-North-Carolina-United-States-of-America/CRA-2--Oncology--IQVIA-Biotech_R1567556","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":"onsite","category":"Healthcare","description":"<p>IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a minimum of 1 year of on-site monitoring experience and oncology solid tumor monitoring experience.</p>\n<p>We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.</p>\n<p><strong>Key Responsibilities</strong></p>\n<ul>\n<li>Conduct all types of site visits,selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.</li>\n<li>Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.</li>\n<li>Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.</li>\n<li>Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.</li>\n<li>Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.</li>\n<li>Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.</li>\n<li>Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.</li>\n<li>Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.</li>\n<li>Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor’s degree in life sciences or health-related field (or equivalent experience).</li>\n<li>Requires at least 1 year of on-site monitoring experience.</li>\n<li>Strong understanding of GCP, ICH guidelines, and regulatory requirements.</li>\n<li>Ability to travel as required by the project.</li>\n</ul>\n<p>The potential base pay range for this role, when annualized, is $74,500.00 - $175,100.00.</p>","enriched_at":1793205264902},{"id":"job_31c73343-b76","title":"Senior Site Contracts Associate","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Sofia-Bulgaria/Senior-Site-Contract-Associate---IQVIA-Biotech_R1557731","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":"remote","category":"Healthcare","description":"<p>IQVIA Biotech is seeking a Senior Site Contracts Associate to support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs.</p>\n<p><strong>Job Overview</strong> The successful candidate will be responsible for supporting the delivery of all required start-up contracting activities, including pre-award activities.</p>\n<p><strong>Essential Functions</strong></p>\n<ul>\n<li>Develop simple investigator grant estimates and proposal text to support the proposal development process.</li>\n<li>Utilize and maintain contract and budget templates and contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs.</li>\n<li>Ensure collaboration with sponsors, stakeholders and RSU regions and countries to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.</li>\n<li>Provide specialist operational and financial contracting support to facilitate efficient business development and initiation and maintenance of clinical trials.</li>\n<li>Assist in the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance.</li>\n<li>Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company.</li>\n<li>Ensure overall contracting efficiency and adherence to project timelines and financial goals.</li>\n<li>Comply with contract management and quality standards.</li>\n</ul>\n<p><strong>Qualifications and Skills</strong></p>\n<ul>\n<li>Bachelor&#39;s Degree in life sciences or health care.</li>\n<li>+6 years relevant experience, including demonstrable experience acting as a contract negotiator.</li>\n<li>Relevant sponsor or clinical research organization clinical site contracting experience.</li>\n<li>Good negotiating and communication skills.</li>\n<li>Good interpersonal skills and a strong team player.</li>\n<li>Strong technical writing skills.</li>\n<li>Understanding of regulated clinical trial environment and knowledge of drug development process.</li>\n<li>Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.</li>\n<li>Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards.</li>\n<li>Good organizational and planning skills.</li>\n<li>Strong knowledge of Microsoft Office and e-mail applications.</li>\n<li>Ability to interpret pricing models and to prepare proposals, bid grids and budgets.</li>\n<li>Good understanding of clinical trial contract management.</li>\n<li>Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.</li>\n</ul>","enriched_at":1793164204167},{"id":"job_bd36ad4c-d52","title":"CPM/Sr CPM","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Madrid-Spain/Senior-Clinical-Project-Manager--Oncology---IQVIA-Biotech_R1532843","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>IQVIA Biotech is recruiting for an experienced CPM/Sr CPM to join their respected, well-established team. The successful candidate will have a minimum of 4 years of regional/global CPM experience and a strong background in working on Oncology trials.</p>\n<p>The Clinical Project Management team at IQVIA Biotech focuses on project delivery, productivity, and quality, resulting in strong financial performance and customer satisfaction. As a CPM/Sr CPM, you will be accountable for the execution of clinical studies, setting objectives for the core project team, and effectively communicating and assessing performance.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Executing clinical studies per contract while optimizing speed, quality, and cost of delivery</li>\n<li>Setting objectives for the core project team and assessing performance</li>\n<li>Participating in bid defense presentations and leading smaller, less complex regional studies</li>\n<li>Developing integrated study management plans with the core project team</li>\n<li>Collaborating with other functional groups to support milestone achievement and manage study issues</li>\n<li>Monitoring progress against contract and preparing project information for stakeholders</li>\n<li>Managing risk and contingencies proactively and leading problem-solving efforts</li>\n<li>Achieving project quality by identifying quality risks and issues and implementing corrective action plans</li>\n<li>Serving as primary or backup project contact with customers and owning relationships with key customer contacts</li>\n<li>Building and leading cross-functional project teams and managing project delivery</li>\n<li>Ensuring financial success and forecasting opportunities to accelerate activities</li>\n<li>Identifying changes in scope and managing change control processes</li>\n<li>Providing input to line managers on project team members&#39; performance</li>\n<li>Supporting staff development and mentoring less experienced project team members</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A Bachelor&#39;s degree in Life Sciences or a related field</li>\n<li>5 years of prior relevant experience, including &gt; 1 year of project management experience</li>\n<li>Advanced knowledge of job area, typically obtained through advanced education combined with experience</li>\n<li>Knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements</li>\n<li>Broad protocol knowledge and therapeutic area knowledge in areas such as cardiovascular-metabolic, renal, or obesity</li>\n<li>Good understanding of project financials and experience managing contractual obligations</li>\n<li>Strong written and verbal communication skills, including excellent command of English</li>\n<li>Strong customer service skills and presentation abilities</li>\n<li>Ability to work across geographies and display high awareness and understanding of cultural differences</li>\n</ul>","enriched_at":1793153216180},{"id":"job_4bbf68bf-b96","title":"CPM/Sr CPM","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Warsaw-Poland/Clinical-Project-Manager--IQVIA-Biotech_R1522841","location":"Warsaw","job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>IQVIA Biotech is recruiting for an experienced CPM/Sr CPM to join their respected, well-established team. The successful candidate will have a minimum of 4 years of regional/global CPM experience, with a strong background in working on Cardiovascular, Renal, or Metabolic trials.</p>\n<p>The CPM/Sr CPM will be accountable for the execution of clinical studies, or assigned portions of clinical studies, per contract while optimizing speed, quality, and cost of delivery. Key responsibilities include:</p>\n<ul>\n<li>Setting objectives for the core project team and assessing performance</li>\n<li>Participating in bid defense presentations and leading smaller, less complex regional studies</li>\n<li>Developing integrated study management plans with the core project team</li>\n<li>Collaborating with other functional groups to support milestone achievement and manage study issues</li>\n<li>Monitoring progress against contract and preparing project information for stakeholders</li>\n<li>Managing risk and contingencies proactively and leading problem-solving efforts</li>\n<li>Achieving project quality by identifying quality risks and issues and implementing corrective action plans</li>\n<li>Serving as primary or backup project contact with customers and owning relationships with key customer contacts</li>\n<li>Building and leading cross-functional project teams and managing project delivery</li>\n<li>Ensuring financial success and forecasting opportunities to accelerate activities</li>\n<li>Identifying changes in scope and managing change control processes</li>\n<li>Providing input to line managers on project team members&#39; performance</li>\n<li>Supporting staff development and mentoring less experienced project team members</li>\n</ul>\n<p>The role requires:</p>\n<ul>\n<li>A Bachelor&#39;s degree in Life Sciences or a related field</li>\n<li>5 years of prior relevant experience, including &gt; 1 year of project management experience</li>\n<li>Advanced knowledge of job area, typically obtained through advanced education combined with experience</li>\n<li>Knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements</li>\n<li>Therapeutic area knowledge in Cardiovascular, Metabolic, or Renal would be an advantage</li>\n<li>Good understanding of project financials and contractual obligations</li>\n<li>Strong written and verbal communication skills, including excellent command of English</li>\n<li>Strong customer service skills and presentation abilities</li>\n<li>Ability to work across geographies and display high awareness of cultural differences</li>\n</ul>\n<p>The potential base pay range for this role is zł217,800.00 - zł404,600.00.</p>","enriched_at":1793153213438},{"id":"job_0787520b-2d9","title":"Clinical Research Associate","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Amsterdam-Netherlands/Experienced-Clinical-Research-Associate---IQVIA-Biotech_R1522187","location":"Amsterdam","job_type":"full-time","experience_level":"senior","work_arrangement":"onsite","category":"Healthcare","description":"<p>IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment. The sector we are in is cutting edge for therapies with un-met medical need.</p>\n<p>IQVIA Biotech has an exciting position within its EU Clinical Monitoring team. The Clinical Monitoring department is the largest team within IQVIA Biotech, providing CRA, Clinical Leads, Management and oversight to global clinical studies.</p>\n<p><strong>Please note, for this role you must be based in the Netherlands.</strong></p>\n<p><strong>Basic Functions:</strong> Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA to ensure all monitoring activities are conducted according to study requirements.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Participates in the investigator recruitment process, performing site evaluation visits of potential investigators to evaluate the capability of the site to successfully manage and conduct the clinical study.</li>\n<li>Coordinate activities with the site and internal departments in preparation for the initiation of the study. Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF and EDC system; monitoring activities and study close-out activities.</li>\n<li>Assists in resolving any issues to ensure compliance with site file audits in conjunction with ISS.</li>\n<li>Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs.</li>\n<li>Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory.</li>\n<li>Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification and works with sites to resolve data queries and produce robust data.</li>\n<li>May review protocols, eCRFs, study manuals and other related documents, as requested by the Clinical Trial Manager and/or Lead CRA.</li>\n<li>Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.</li>\n<li>Assists with, and attends, Investigator Meetings for assigned studies.</li>\n<li>Attends study-related, company, departmental, and external meetings, as required.</li>\n<li>Ensures all study deliverables are completed per IQVIA Biotech and study timelines</li>\n<li>Conducts Field Evaluation Visits and field training of CRA Is, IIs and other Sr. CRAs.</li>\n<li>Serves as mentor for junior CRAs and those new to the company and/or study.</li>\n</ul>\n<p><strong>KNOWLEDGE, SKILLS AND ABILITIES:</strong></p>\n<ul>\n<li>Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology.</li>\n<li>Minimum of 1-2 years of onsite monitoring experience is a must.</li>\n<li>Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.</li>\n<li>Able to form productive professional relationships both internally within own function, cross-functionally and externally with health care professionals.</li>\n<li>Able to handle several priorities within multiple, complex trials.</li>\n<li>Able to reason independently and recommend specific solutions in clinical settings.</li>\n<li>Able to work independently, prioritize, and work within a matrix team environment.</li>\n<li>Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research.</li>\n<li>Candidates must have strong communication levels of Dutch and English.</li>\n</ul>","enriched_at":1793149305114},{"id":"job_377cef67-585","title":"Clinical Research Associate (CRA) 2","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Buenos-Aires-Argentina/CRA-2--Argentina--IQVIA-Biotech_R1540400","location":"Buenos Aires","job_type":"full-time","experience_level":"mid","work_arrangement":"onsite","category":"Healthcare","description":"<p>IQVIA Biotech is seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials.</p>\n<p>In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations.</p>\n<p><strong>Key Responsibilities</strong></p>\n<ul>\n<li>Conduct all types of site visits,selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.</li>\n<li>Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.</li>\n<li>Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.</li>\n<li>Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.</li>\n<li>Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.</li>\n<li>Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.</li>\n<li>Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.</li>\n<li>Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.</li>\n<li>Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor’s degree in life sciences or health-related field (or equivalent experience).</li>\n<li>Requires at least 1 year of on-site monitoring experience.</li>\n<li>Strong understanding of GCP, ICH guidelines, and regulatory requirements.</li>\n<li>Ability to travel as required by the project.</li>\n</ul>","enriched_at":1793147107592}],"category_normalised":[{"category":"healthcare","count":24},{"category":"research","count":1}],"velocity":{"weeks":[{"week_start":"2026-10-19","count":3},{"week_start":"2026-10-26","count":22}],"trend":"stable","wow_pct":633},"momentum":{"recent_14d":25,"prior_14d":0,"growth_pct":0,"classification":"stable"},"salary_vs_industry":{"company_median":150950,"industry_median":null,"percentile":null,"sample_size":8,"by_region":[{"region":"Unknown","company_median":151300,"industry_median":null,"sample":7}],"transparency_pct":32,"industry_transparency_pct":0,"transparency_warning":false},"market_share":{"company_jobs":25,"industry_total":25,"share_pct":100,"rank":1,"peer_count":1},"ai_exposure":{"occupation_weighted_score":0.172,"skill_weighted_score":0.193,"top_exposed_titles":[{"title":"Senior Clinical Research Associate (Sr CRA 3)","count":2,"score":0.245}],"top_exposed_skills":[{"skill":"ICH 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