714 matching jobs for “Senior Clinical Research Associate”

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Thermo Fisher Scientific

Sr CRA (Level I) - FSP

Remote, Chile

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 21, 2026

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Thermo Fisher Scientific

Sr CRA (Level I) - FSP

Remote, Argentina +1 location 2 postings

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Sr CRA (Level I) - FSP

Remote, Mexico

Descripción de puesto Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Gilead Sciences

Sr Manager, Biostatistics

Foster City, California, United States

Full time
Regular

Pay posted by employer$169,320–$219,120

… Education & Experience Requirements: Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project …

Added Oct 16, 2026

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Danaher

Senior Quality Engineer

Chaska, Minnesota, United States

Regular

… improvement, you help turn ideas into impact – innovating at the speed of life. As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory’s …

Added Oct 15, 2026

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IQVIA Holdings

Sr. CRA 3, Brazil, IQVIA Biotech

São Paulo, Brazil

… partnerships that help bring breakthrough treatments to patients faster. We are seeking an experienced Senior Clinical Research Associate (Sr CRA 3) to join our Clinical Monitoring team in Brazil. In this role, you will independently manage and …

Added Oct 15, 2026

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IQVIA Holdings

Sr. CRA 3, Argentina, IQVIA Biotech

Buenos Aires, Argentina

… partnerships that help bring breakthrough treatments to patients faster. We are seeking an experienced Senior Clinical Research Associate (Sr CRA 3) to join our Clinical Monitoring team in Argentina. In this role, you will independently manage …

Added Oct 15, 2026

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Thermo Fisher Scientific

Senior CRA level II

Prague, Prague, Czechia

… to perform and coordinate all aspects of the clinical monitoring and site management process. As a Senior Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage …

Added Oct 16, 2026

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Amgen

Sr Mgr Centralized Study Support

India - Hyderabad

Full time
Regular

… Study Support (CSS). This role ensures delivery of high ‑ quality centralized operational support across clinical programs and alignment of resources with organizational priorities. Roles & Responsibilities: Team …

Added Oct 15, 2026

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Danaher

Senior Technician Facilities Management

Hialeah, Florida, United States

Regular

Added Oct 15, 2026

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IQVIA Holdings

Associate Medical Director, Medical & Scientific Communications

Red Bank, NJ, United States of America

Pay posted by employer$109,400–$304,900

… and medical writers, fostering a culture of excellence, accountability, and professional growth. Serve as a senior scientific advisor to clients, building trusted partnerships and shaping medical communication strategies …

Added Oct 15, 2026

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Becton Dickinson

Associate Director of Market Access & Payer Strategy

USA FL - Stuart Airport Road

Remote
Full time
Regular

Associate Director, Market Access & Payer Strategy Liberator Medical Supply (BD Urology & Critical Care) Location: …

Added Oct 27, 2026

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Thermo Fisher Scientific

FSP Sr CRA (Level I)

Remote, Mexico

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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IQVIA Holdings

Associate Solution and Delivery Lead, Healthcare & Pharma

Basel, Switzerland +1 location

… within key accounts, identifying and advancing cross-selling and upselling opportunities. Build and sustain senior-level (typically HQ-level) client relationships beyond active engagements to support early positioning and …

Added Oct 15, 2026

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Thermo Fisher Scientific

FSP Sr CRA (Level I)

Remote, Mexico

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Bristol-Myers Squibb

Sr. Scientist, Radiopharmaceuticals

Indianapolis - RayzeBio - IN

Full time
Regular

Pay posted by employer$107,904–$130,754

… for preclinical development of radiopharmaceuticals. · Drive CMC process development and optimization for clinical drug products, including formulation lock and robust process definition, ensuring scalability and …

Added Oct 15, 2026

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Abbott Laboratories

Senior Manager Medical Affairs

Mumbai, Maharashtra, India

… Medical Affairs Sub-Function, supervises professionals in overseeing the direction, planning, execution, clinical trials/research and the data collection activities. • Contributes to implementation of clinical protocols, …

Added Oct 30, 2026

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IQVIA Holdings

Sr Production Assoc

Taguig City, Philippines

… to ensure it accurately reflects the actual / closest invoice details. • Escalates issues to Team Lead or Associate Manager. List of required skills for this role: • Ability to read and translate paper invoice details. • …

Added Oct 15, 2026

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IQVIA Holdings

Associate Director, Client Services - IQVIA Medical Communications

Reading, United Kingdom +1 location

… of Practice to identify opportunities to cross sell solutions and extend relationships with clients from clinical study support into Medical Affairs Communications Accountable for ensuring accurate forecasting, invoicing, …

Added Oct 15, 2026

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Johnson & Johnson

Health Economics & Market Access Associate Director

Prague, Czechia +1 location

Full time
Regular

… breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/. Senior Manager, Health Economics & Market Access (HEMA), Emerging Markets CEE Location: Prague or Warsaw Contract: …

Added Oct 15, 2026

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Thermo Fisher Scientific

Sr CRA (Level I) - FSP

Remote, Chile

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About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Senior Clinical Research Associate (Level I), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You’ll Do:
• Monitors investigator sites with a risk-based monitoring approach: applies rootcause analysis (RCA), critical thinking and problem-solving skills to identify siteprocesses failure and corrective/preventive actions to bring the site intocompliance and decrease risks. Ensures data accuracy through SDR, SDV andCRF review as applicable through on-site and remote monitoring activities.Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable
• Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required.
• Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.
• Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
• Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).
• Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
• Responds to company, client and applicable regulatory requirements/audits/inspections.
• Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
• Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:

• Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic/vocational qualification.
• Previous experience that provides the knowledge, skills, and abilities to perform the job, including:
– A minimum of 3 years of completed on-site clinical monitoring experience.
– A minimum of 2 years of completed experience as the lead Clinical Research Associate (CRA) on Oncology and/or Hematology clinical trials.

Knowledge, Skills and Abilities:
• Effective clinical monitoring skills
• Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
• Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents
• Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
• Ability to manages Risk Based Monitoring concepts and processes
• Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
• Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues
• Effective interpersonal skills
• Strong attention to detail
• Effective organizational and time management skills
• Ability to remain flexible and adaptable in a wide range of scenarios
• Ability to work in a team or independently as required
• Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software
• Good English language and grammar skills
• Good presentation skills

Working Conditions and Environment:
• Working Conditions and Environment:
• Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
• Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals.
• May also include extended overnight stays.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Personal protective equipment required such as protective eyewear, garments and gloves.
• Exposure to fluctuating and/or extreme temperatures on rare occasions.
• Must be able to comply with specific sponsor/client/site requirements, even if not required by Thermo Fisher Scientific (e.g., disclosure of vaccination status, or other personal information). On some occasions, this information may be required to be provided directly to sponsor/client/site.

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