{"data":{"company":{"name":"Syneos Health","slug":"syneos-health","logo_url":"https://logos.yubhub.co/syneoshealth.com.png","canonical_domain":"syneoshealth.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":43,"categories":[{"category":"healthcare","count":29},{"category":"product management","count":2},{"category":"operations","count":2},{"category":"human resources","count":2},{"category":"finance","count":2},{"category":"data science","count":2},{"category":"consulting","count":2},{"category":"other","count":1},{"category":"legal","count":1}],"experience_levels":[{"level":"senior","count":27},{"level":"mid","count":7},{"level":"entry","count":3}],"work_arrangements":[{"arrangement":"hybrid","count":5},{"arrangement":"remote","count":4},{"arrangement":"onsite","count":1}],"top_titles":[{"title":"Vendor/Tech/Life Sciences Counsel I","count":1},{"title":"Sr. Biostatistician_Clinpharm","count":1},{"title":"Sr CRA I/II - 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Single Sponsor","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ROU-Client/CRA-II---Single-Sponsor---Based-in-Bucharest_25100863","location":"Bucharest","job_type":"full-time","experience_level":"senior","work_arrangement":"hybrid","category":"Healthcare","description":"<p>Syneos Health is seeking a CRA II - Single Sponsor based in Bucharest. As a CRA II, you will conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Conduct on-site and remote monitoring of clinical research studies</li>\n<li>Develop and implement tools, procedures, and processes to ensure quality monitoring</li>\n<li>Contribute to the design, implementation, and delivery of processes, programs, and policies</li>\n<li>Manage defined components of projects or processes within the area of responsibility</li>\n<li>Ensure accurate and timely documentation of monitoring activities and findings</li>\n<li>Collaborate with cross-functional teams to support clinical trial operations</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree in a related field or equivalent experience</li>\n<li>Minimum of 2-4 years of experience in clinical research monitoring</li>\n<li>Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements</li>\n<li>Excellent communication and interpersonal skills</li>\n<li>Ability to work independently and manage multiple priorities</li>\n<li>Proficiency in using clinical trial management systems and other relevant software</li>\n</ul>\n<p>Certifications:</p>\n<ul>\n<li>Certified Clinical Research Associate (CCRA) or equivalent certification preferred</li>\n</ul>\n<p>Necessary Skills:</p>\n<ul>\n<li>Attention to detail and strong analytical skills</li>\n<li>Problem-solving abilities and critical thinking</li>\n<li>Ability to work effectively in a team environment</li>\n<li>Strong organizational and time management skills</li>\n<li>Proficiency in Microsoft Office Suite</li>\n</ul>","enriched_at":1793018860821},{"id":"job_45458200-758","title":"CRA II - Sr.CRA I for FSP BU, South Korea","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/KOR-Remote/SrCRA-II-for-FSP-BU--South-Korea_25111534","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":"hybrid","category":"Healthcare","description":"<p>Syneos Health is seeking a CRA II - Sr.CRA I for FSP BU, South Korea.</p>\n<p>The Clinical Research Associate (CRA) will play a crucial role in ensuring the quality and integrity of clinical trials. The successful candidate will be responsible for performing site qualification, site initiation, interim monitoring, site management, and close-out visits.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Conducting site qualification, site initiation, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance</li>\n<li>Evaluating the overall performance of site staff and providing recommendations for site-specific actions</li>\n<li>Verifying the process of obtaining informed consent from subjects/patients</li>\n<li>Assessing factors that might affect subject/patient safety and clinical data integrity</li>\n<li>Conducting source document reviews and verifying required clinical data entered in case report forms</li>\n<li>Applying query resolution techniques and providing guidance to site staff</li>\n<li>Managing site-level activities and communication to ensure project objectives, deliverables, and timelines are met</li>\n<li>Preparing for and attending investigator meetings and sponsor face-to-face meetings</li>\n<li>Providing guidance at the site and project level towards audit readiness standards</li>\n<li>May act as primary liaison with study site personnel or in collaboration with Central Monitoring Associate</li>\n<li>May provide direct supervision, training, and/or mentorship to more junior level CRAs</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p>Syneos Health offers a dynamic and supportive work environment, opportunities for career development and progression, and a range of benefits to support employees.</p>","enriched_at":1793018694896},{"id":"job_c009490b-be1","title":"Clin Ops Specialist","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client/COS_25101452","location":"Shanghai","job_type":"full-time","experience_level":"mid","work_arrangement":null,"category":"Healthcare","description":"<p>Syneos Health is seeking a Clin Ops Specialist to join their team in Shanghai or Guangzhou. As a Clin Ops Specialist, you will play a crucial role in safeguarding the wellbeing of research subjects, reviewing study protocols, and ensuring compliance with regulatory standards.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Safeguard the wellbeing of research subjects in a medical capacity, ensuring that all procedures are conducted with the highest standards of care and safety</li>\n<li>Review study protocols and execute procedures in alignment with protocols and regulatory, health, and safety standards</li>\n<li>Recruit and coordinate communication with clinical trial volunteers and patients, maintaining clear and effective communication throughout the study</li>\n<li>Follow applicable regulations globally and by region, ensuring that all activities are conducted in accordance with local and international standards</li>\n<li>Collaborate with cross-functional teams to develop study materials, including informed consent forms, study manuals, and other essential documents</li>\n<li>Monitor trial progress and address any issues that arise during the study</li>\n<li>Provide organizational related support or service, typically under supervision, assisting with administrative tasks and other support activities as needed</li>\n<li>Perform routine tasks with some deviation from standard practice, adapting to changing circumstances and requirements as necessary</li>\n<li>Utilize broad knowledge of operational systems and practices gained through extensive experience and/or education, applying this knowledge to improve study processes and outcomes</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>High school diploma or equivalent required</li>\n<li>Associate&#39;s degree or higher in a related field preferred</li>\n<li>Minimum of 2 years of experience in clinical operations or a related field</li>\n<li>Strong understanding of clinical research protocols and regulatory requirements</li>\n</ul>\n<p><strong>Certifications</strong></p>\n<ul>\n<li>Certified Clinical Research Coordinator (CCRC) or equivalent certification preferred</li>\n<li>Basic Life Support (BLS) certification required</li>\n</ul>\n<p><strong>Necessary Skills</strong></p>\n<ul>\n<li>Excellent communication and interpersonal skills</li>\n<li>Strong organizational and time management abilities</li>\n<li>Attention to detail and accuracy in documentation</li>\n<li>Ability to work effectively in a team environment</li>\n<li>Proficiency in Microsoft Office Suite and clinical trial management software</li>\n</ul>","enriched_at":1793015246680},{"id":"job_d354e1db-57c","title":"Project Manager II","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/GBR-London-Hybrid/Project-Manager-II---3-days-a-week-in-Uxbridge_25101432","location":"Uxbridge","job_type":"part-time","experience_level":"senior","work_arrangement":"onsite","category":"Healthcare","description":"<p>Syneos Health is seeking a Project Manager II to work 3 days a week in Uxbridge.</p>\n<p>As a Project Manager II, you will plan, direct, create, and communicate clinical study timelines to ensure deliverables are produced on schedule. You will gather input from cross-functional teams to create comprehensive plans for clinical studies and ensure consistency of clinical study processes across clinical trials.</p>\n<p>Key responsibilities:</p>\n<ul>\n<li>Plan and manage clinical study timelines</li>\n<li>Collaborate with cross-functional teams to integrate their feedback into study plans</li>\n<li>Ensure consistency of clinical study processes across trials</li>\n<li>Oversee and resolve operational aspects of clinical trials</li>\n<li>Select sites and vendors, prepare clinical trial budgets</li>\n<li>Monitor progress and follow up with team members and line managers</li>\n<li>Implement and prepare clinical development strategies</li>\n<li>Develop trial recruitment strategies</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s degree in a related field (e.g., Clinical Research, Life Sciences, Healthcare Management)</li>\n<li>Minimum of 5 years of experience in clinical project management or a related role</li>\n<li>Proven track record of successfully managing clinical trials</li>\n<li>Certification in Clinical Research (e.g., CCRP, CCRA) is preferred</li>\n<li>Project Management Professional (PMP) certification is a plus</li>\n</ul>\n<p>Necessary skills:</p>\n<ul>\n<li>Strong organizational and planning skills</li>\n<li>Excellent communication skills</li>\n<li>Ability to oversee and resolve operational aspects of clinical trials</li>\n<li>Knowledge of SOP, GCP, and country regulations</li>\n<li>Experience in site and vendor selection, budget preparation, and monitoring progress</li>\n<li>Strong problem-solving skills</li>\n</ul>","enriched_at":1793015245384},{"id":"job_34976614-2ff","title":"Site Contracts Specialist","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ARG-Remote/Site-Contracts-Specialist-with-experience-in-Clinical-Trials--Home-Based-Mexico--Brazil-and-Argentina_25100444","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":"remote","category":"Healthcare","description":"<p>Syneos Health is seeking a Site Contracts Specialist with experience in Clinical Trials. As a Site Contracts Specialist, you will lead multi-country projects, negotiate and prepare contracts, budgets, and related documents for participation in industry-sponsored clinical trials.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Lead multi-country projects including negotiating and preparing contracts, budgets, and related documents for participation in industry-sponsored clinical trials.</li>\n<li>Produce site-specific contracts from country clinical trial agreement (CTA) template.</li>\n<li>Negotiate budget and contract with site and via Site Contracts Service Centre and SSUL with Sponsor until resolution of issues.</li>\n<li>Perform quality control and arrange execution of CTAs as well as archival of documents into repositories and capture of metadata.</li>\n<li>Administer all contract management processes, including coordination with relevant protocol, informed consent, institution, investigator, vendor, consultant, and customer agreement documents at a project level.</li>\n<li>Generate amended contract and/or budget documents as necessary.</li>\n<li>Work closely with Site Contract Service Center and Legal to harmonize site contract to reflect sponsor&#39;s master service agreement terms.</li>\n<li>Identify possible contract or process operational risk and proactively work within the team to provide solutions.</li>\n<li>Provide support to business development and represent site contracts/Site Start-Up (SSU) at internal or customer meetings.</li>\n<li>Collaborate with internal and external legal, finance, and clinical operations departments.</li>\n<li>Maintain and actively support review and development of contract templates, budget templates and site specific files and databases.</li>\n<li>Serve as key communication liaison between site contracts staff and internal and external customers.</li>\n<li>Train and mentor less experienced staff members on departmental Standard Operating Procedures (SOPs).</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>BA/BS degree in Business Administration, Public Administration, Public Health, related field, or equivalent combination of education and experience.</li>\n<li>Moderate contracts management experience that includes experience in a contract research organization or pharmaceutical industry.</li>\n<li>Strong knowledge of the clinical development process and legal and contracting parameters.</li>\n<li>Strong computer skills in Microsoft Office Suite.</li>\n<li>Customer focused and ability to manage challenging priorities and to remain flexible and adaptable in stressful situations.</li>\n<li>Excellent understanding of clinical trial process across Phases II-IV and ICH GCP.</li>\n<li>Good understanding clinical protocols and associated study specifications.</li>\n<li>Excellent understanding of clinical trial start-up processes.</li>\n<li>Project management experience in a fast-paced environment.</li>\n<li>Good vendor management skills.</li>\n<li>Strong organizational skills with proven ability to handle multiple projects.</li>\n<li>Excellent communication, presentation and interpersonal skills.</li>\n<li>Quality-driven in all managed activities.</li>\n<li>Strong negotiating skills.</li>\n<li>Strong problem-solving skills.</li>\n<li>Ability to mentor and motivate more junior staff.</li>\n</ul>\n<p>Benefits: Syneos Health offers a comprehensive benefits package, including career development and progression, supportive and engaged line management, technical and therapeutic area training, peer recognition, and total rewards program.</p>\n<p>Salary: The annual base salary for this position ranges from $56,000 to $95,000.</p>","enriched_at":1793015243848},{"id":"job_8a652544-c31","title":"Sr CRA I/II - Sweden, Sponsor-dedicated (Pipeline)","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/SWE-Remote/Sr-CRA-I-II---Sweden--Sponsor-dedicated--Pipeline-_25101241","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>Syneos Health is seeking a Sr CRA I/II - Sweden, Sponsor-dedicated (Pipeline). As a Sr CRA, you will play a critical role in ensuring the quality and compliance of clinical trials.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices</li>\n<li>Develop and implement tools, procedures, and processes to ensure quality monitoring</li>\n<li>Contribute to the design, implementation, and delivery of processes, programs, and policies</li>\n<li>Manage and direct the work of lower-level professionals or manage processes and programs</li>\n<li>Ensure accurate and timely documentation and reporting of clinical trial data</li>\n<li>Collaborate with cross-functional teams to support clinical trial activities</li>\n<li>Identify and resolve issues related to clinical trial conduct and data integrity</li>\n<li>Provide training and mentorship to junior staff members</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in a related field</li>\n<li>Minimum of 3-5 years of experience in clinical research or a related field</li>\n<li>In-depth knowledge of clinical trial processes and regulations</li>\n<li>Strong analytical and problem-solving skills</li>\n<li>Excellent communication and interpersonal skills</li>\n<li>Ability to work independently and as part of a team</li>\n</ul>\n<p><strong>Certifications</strong></p>\n<ul>\n<li>Certified Clinical Research Professional (CCRP) or equivalent certification preferred</li>\n</ul>\n<p><strong>Necessary Skills</strong></p>\n<ul>\n<li>Proficiency in clinical trial management systems and software</li>\n<li>Strong organizational and time management skills</li>\n<li>Attention to detail and accuracy</li>\n<li>Ability to manage multiple projects and priorities simultaneously</li>\n<li>Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements</li>\n</ul>","enriched_at":1793015240667},{"id":"job_2e078693-d8a","title":"CRA II/ Sr CRA - Poland, Sponsor -dedicated (Pipeline)","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/POL-Remote/CRA-II--Sr-CRA---Poland--Sponsor--dedicated---Pipeline-_25101236","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>Syneos Health is seeking a CRA II/ Sr CRA - Poland, Sponsor -dedicated (Pipeline). As a CRA II/ Sr CRA, you will conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Conduct on-site and remote monitoring of clinical research studies</li>\n<li>Develop and implement tools, procedures, and processes to ensure quality monitoring</li>\n<li>Contribute to the design, implementation, and delivery of processes, programs, and policies</li>\n<li>Manage and direct the work of lower-level professionals or manage processes and programs</li>\n<li>Ensure accurate and timely documentation and reporting of clinical trial data</li>\n<li>Collaborate with cross-functional teams to support clinical trial activities</li>\n<li>Identify and resolve issues related to clinical trial conduct and data integrity</li>\n<li>Provide training and mentorship to junior staff members</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree in a related field</li>\n<li>Minimum of 3-5 years of experience in clinical research or a related field</li>\n<li>In-depth knowledge of clinical trial processes and regulations</li>\n<li>Strong analytical and problem-solving skills</li>\n<li>Excellent communication and interpersonal skills</li>\n<li>Ability to work independently and as part of a team</li>\n</ul>\n<p>Certifications:</p>\n<ul>\n<li>Certified Clinical Research Professional (CCRP) or equivalent certification preferred</li>\n</ul>\n<p>Necessary Skills:</p>\n<ul>\n<li>Proficiency in clinical trial management systems and software</li>\n<li>Strong organizational and time management skills</li>\n<li>Attention to detail and accuracy</li>\n<li>Ability to manage multiple projects and priorities simultaneously</li>\n<li>Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements</li>\n</ul>","enriched_at":1793015239380},{"id":"job_ecfae914-116","title":"Medical Writer I (CTT)","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/IND-Remote/Medical-Writer-I--CTT-_25000363","location":null,"job_type":"full-time","experience_level":"entry","work_arrangement":null,"category":"Healthcare","description":"<p>Syneos Health is seeking a Medical Writer I (CTT) to join their team. The successful candidate will serve as a medical writer on clinical study or regulatory project teams, assisting in writing, editing, and coordinating content for clinical/regulatory documents.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Compiles, writes, and edits medical writing deliverables, serving as a medical writer within and across departments with moderate supervision.</li>\n<li>Develops or supports various documents, including:</li>\n<li>Clinical study protocols and amendments</li>\n<li>Clinical study reports</li>\n<li>Patient narratives</li>\n<li>Investigator brochures</li>\n<li>Reviews statistical analysis plans and table/figure/listing specifications for content, grammar, format, and consistency.</li>\n<li>Interacts with department heads and staff members in data management, biostatistics, regulatory affairs, and medical affairs to produce writing deliverables.</li>\n<li>Adheres to established regulatory standards, including ICH-E3 guidelines and Company Standard Operating Procedures.</li>\n<li>Performs online clinical literature searches as applicable.</li>\n<li>Continues professional development to keep pace with regulatory guidance and client expectations.</li>\n<li>Is aware of budget specifications for assigned projects, working within budgeted hours and communicating changes to medical writing leadership.</li>\n<li>Completes required administrative tasks within specified timeframes.</li>\n<li>Performs other work-related duties as assigned, with minimal travel (less than 25%).</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>Minimum 1 year of experience in clinical trial disclosure or CTT.</li>\n<li>Good experience in protocol registration and result registration.</li>\n<li>Experience with results posting for regulatory bodies.</li>\n</ul>\n<p><strong>What We Offer</strong></p>\n<ul>\n<li>Career development and progression opportunities</li>\n<li>Supportive and engaged line management</li>\n<li>Technical and therapeutic area training</li>\n<li>Peer recognition and total rewards program</li>\n<li>Total Self culture, allowing you to authentically be yourself</li>\n</ul>","enriched_at":1793014892099},{"id":"job_eb19687d-9bd","title":"CRA II - Sponsor dedicated - Argentina","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ARG-Buenos-Aires/CRA-II---Sponsor-dedicated---Argentina_25102243","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":"hybrid","category":"Healthcare","description":"<p>Syneos Health is seeking a CRA II - Sponsor dedicated - Argentina. The successful candidate will perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits</li>\n<li>Evaluate overall performance of site and site staff and provide recommendations regarding site-specific actions</li>\n<li>Verify process of obtaining informed consent has been adequately performed and documented for each subject/patient</li>\n<li>Assess factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site</li>\n<li>Conduct Source Document Review of appropriate site source documents and medical records</li>\n<li>Verify required clinical data entered in the case report form (CRF) is accurate and complete</li>\n<li>Apply query resolution techniques remotely and on site, and provide guidance to site staff as necessary</li>\n<li>Utilize available hardware and software to support the effective conduct of the clinical study data review and capture</li>\n<li>Verify site compliance with electronic data capture requirements</li>\n<li>Perform investigational product (IP) inventory, reconciliation, and reviews storage and security</li>\n<li>Routinely review the Investigator Site File (ISF) for accuracy, timeliness, and completeness</li>\n<li>Document activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents</li>\n<li>Support subject/patient recruitment, retention, and awareness strategies</li>\n<li>Enter data into tracking systems as required to track all observations, ongoing status, and assigned action items to resolution</li>\n<li>Understand project scope, budgets, and timelines; manage site-level activities/communication to ensure project objectives, deliverables, and timelines are met</li>\n<li>Act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate</li>\n<li>Prepare for and attend Investigator Meetings and/or sponsor face-to-face meetings</li>\n<li>Provide guidance at the site and project level towards audit readiness standards and support preparation for audit and required follow-up actions</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Good computer skills and ability to embrace new technologies</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>","enriched_at":1793014890036},{"id":"job_285db4cf-e53","title":"Sample Management Specialist II","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ARG-Remote/Sample-Management-Specialist-II---Experience-with-end-to-end-sample-management-process---Argentina-Home-Based_25102030","location":null,"job_type":"full-time","experience_level":"mid","work_arrangement":"remote","category":"Operations","description":"<p>Syneos Health is seeking a Sample Management Specialist II to work remotely from Argentina.</p>\n<p>The Sample Management Specialist II is responsible for managing samples, including receipt, inventory, chain of custody, storage, transfers, and disposition. The ideal candidate will have experience with end-to-end sample management processes and be skilled in operating and troubleshooting storage appliances and environmental monitoring systems.</p>\n<p><strong>Core Responsibilities</strong></p>\n<ul>\n<li>Receive, control, and dispose of study samples and reference materials</li>\n<li>Manage shipping and receiving samples, including destruction and transfer as directed by clients</li>\n<li>Provide samples and materials to laboratory staff for analysis</li>\n<li>Maintain inventory of supplies and order new supplies as needed</li>\n<li>Assist with maintenance, operation, and support of sample storage equipment and monitoring systems</li>\n<li>Archive documents related to sample management</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>High school diploma</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Good computer skills, including Microsoft Word and Excel</li>\n<li>Ability to use sample-tracking software</li>\n<li>Bilingualism in English and Spanish, with understanding of simple messages and basic instructions</li>\n</ul>\n<p><strong>What We Offer</strong></p>\n<p>Syneos Health offers a range of benefits, including career development and progression, supportive line management, technical and therapeutic area training, and total rewards programs.</p>","enriched_at":1793014887890}],"category_normalised":[{"category":"healthcare","count":29},{"category":"product management","count":2},{"category":"operations","count":2},{"category":"human resources","count":2},{"category":"finance","count":2},{"category":"data science","count":2},{"category":"consulting","count":2},{"category":"legal","count":1}],"velocity":{"weeks":[{"week_start":"2026-10-19","count":43}],"trend":"stable","wow_pct":0},"momentum":{"recent_14d":43,"prior_14d":0,"growth_pct":0,"classification":"stable"},"salary_vs_industry":{"company_median":80625,"industry_median":null,"percentile":null,"sample_size":2,"by_region":[{"region":"Unknown","company_median":80625,"industry_median":null,"sample":2}],"transparency_pct":5,"industry_transparency_pct":0,"transparency_warning":true},"market_share":{"company_jobs":43,"industry_total":43,"share_pct":100,"rank":1,"peer_count":1},"ai_exposure":{"occupation_weighted_score":0.299,"skill_weighted_score":0.312,"top_exposed_titles":[],"top_exposed_skills":[{"skill":"Excel","count":3,"score":0.372},{"skill":"Microsoft Excel","count":3,"score":0.252}]},"peer_set":[],"skills_lq":[],"geographic_shift":{"current":[{"region":"Unknown","count":3,"share_pct":42.9},{"region":"APAC","count":3,"share_pct":42.9},{"region":"Latin America","count":1,"share_pct":14.3}],"emerging":[{"region":"Unknown","recent_30d":3,"prior_30d":0,"growth_pct":100},{"region":"APAC","recent_30d":3,"prior_30d":0,"growth_pct":100}],"shrinking":[]},"seniority_anomalies":{"exec_recent_30d":1,"exec_prior_90d_avg":0,"exec_growth_pct":100,"notable_exec_hires":[{"title":"Associate Director (Deal management products- Salesforce/Oracle APEX)","location":null,"posted_at":"2026-10-26"}]},"posting_dynamics":{"median_days_open":null,"industry_median_days_open":null,"long_open_count":0,"closure_rate_pct":0}}}}