1,000+ matching jobs for “Clinical Research Associate”

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Thermo Fisher Scientific

CRA Level I

Remote, Hungary

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

Added Nov 5, 2026

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IQVIA Holdings

Assistente Administrativo de Pesquisa Clínica - Exclusivo para Pessoas com Deficiência

São Paulo, Brazil

… vacancies within IQVIA jobs. Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File …

Added Oct 15, 2026

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IQVIA Holdings

Sr. CRA, Oncology, IQVIA Biotech

Durham, North Carolina, United States +3 locations

Pay posted by employer$105,100–$197,500

… to patients faster. Hiring Senior Clinical Research Associates We are seeking an experienced Senior Clinical Research Associate to join our Clinical Monitoring team. In this role, you will independently manage and monitor clinical …

Added Oct 15, 2026

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IQVIA Holdings

Site Enablement Lead & Site Facing Line Manager

Istanbul, Turkey

… Willingness to travel within Turkey as required. Preferred Experience Clinical Research Coordinator (CRC), Clinical Research Associate (CRA), Site Manager, Study Coordinator, or similar background. Experience supporting patient recruitment or …

Added Oct 15, 2026

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Pfizer

Analista de Pesquisa Clínica Jr

São Paulo, São Paulo, Brazil

Full time
Regular

Responsible for investigator site management and monitoring for assigned sites: Clinical Trial Monitoring • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan …

Added Oct 16, 2026

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IQVIA Holdings

CRA II or SrCRA I (m/w/d), Single Sponsor, home-based Austria

Vienna, Austria

… the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Managing progress by tracking …

Added Oct 15, 2026

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IQVIA Holdings

Intern in Site Management department - Serbia

Belgrade, Serbia

… work. When the Internship is successfully finished, the Intern should have a good overview of the world of Clinical Trials, CRA and CSA job responsibilities and be ready for their next career step. Qualifications: …

Added Oct 15, 2026

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Thermo Fisher Scientific

CRA II/ Sr CRA I/ Sr CRA II - US Southeast Region - Multiple Therapeutic Areas Available

Remote, Florida, USA

Job Description Join Us as a Clinical Research Associate (Level II) – 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

CRA 2/Senior CRA 1

San Juan, Puerto Rico

Pay posted by employer$76,300–$175,100

… or a related field (or equivalent experience). Minimum of 1.5 years of on-site monitoring experience as a Clinical Research Associate. Fluency in both English and Spanish (written and verbal) required. Experience monitoring studies in CNS, …

Added Oct 15, 2026

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IQVIA Holdings

CTA

Chengdu, China

Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining …

Added Oct 15, 2026

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IQVIA Holdings

Senior CRA

Buenos Aires, Argentina

… a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. REQUIREMENTS You should have: A Bachelor's degree in a health care or …

Added Oct 15, 2026

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Thermo Fisher Scientific

CRA II/Sr CRA - Sponsor-Dedicated FSP - Germany (m/f/d)

Remote, Germany

… degree in a life sciences related field or equivalent qualification Minimum 2 + years of experience as a Clinical Research Associate / Monitor Valid driver’s license Full right to work in Germany Fluency in German and English (C1 level) – …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP - CRA I - South Africa

Remote, South Africa

Job Description Join Us as an FSP Clinical Research Associate Level I – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Nov 4, 2026

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Thermo Fisher Scientific

Medical Director/Senior Medical Director Rheumatology (Client dedicated)

Remote, Argentina

Join Us as an Associate Medical Director – Make an Impact at the Forefront of Innovation At Thermo Fisher Scientific, you’ll …

Added Oct 16, 2026

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IQVIA Holdings

Freelance CRA - Czech Republic

Prague, Czech Republic

Join IQVIA Biotech as a Freelance Clinical Research Associate supporting two Phase III Oncology clinical trials. You’ll lead site visits, monitor compliance, and ensure …

Added Oct 15, 2026

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IQVIA Holdings

Sr. CRA 3, Brazil, IQVIA Biotech

São Paulo, Brazil

… 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

… 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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Johnson & Johnson

Lead Local Trial Manager

Mumbai, India

… Local Trial Manager is considered as a senior trial management role with at least 14+ years of overall clinical trial experience: 4+ years of clinical trial management experience & more than 6 years of clinical …

Added Oct 15, 2026

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Thermo Fisher Scientific

Data Compliance Coordinator

Birmingham, England, United Kingdom

… find cures for cancer. DESCRIPTION: Join our team at Thermo Fisher Scientific as a Corporate Compliance Associate II supporting clinical trials across our research sites. In this role, you'll ensure data quality and …

Added Oct 22, 2026

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IQVIA Holdings

Local Trial Manager (Sponsor Dedicated)

Durham, North Carolina, United States

Pay posted by employer$68,400–$232,800

Job Overview Associate Project Leads (Local Trial Managers) are an integral part of clinical trial delivery, liaising with …

Added Oct 15, 2026

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Pfizer

Analista de Pesquisa Clínica Jr

São Paulo, São Paulo, Brazil

Full time
Regular

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QUALIFICATIONS · employer excerpt

Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
Knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations
Monitoring Experience: Minimum 1-year relevant experience in clinical research site monitoring and management
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience preferred

1 more in the full description below.

About this opportunity

Original employer description

The Clinical Research Associate is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices, and Pfizer standards.

The Clinical Research Associate role is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (e.g. enrollment, database release), to safeguard the quality of investigator sites (e.g. patient safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and satisfaction, and to enhance the company’s image with its external stakeholders.

The Clinical Research Associate is responsible for the resolution of all protocol-related issues for assigned investigator sites and will work closely with the Site Care Partner, and other members of the study team, as required, in activities associated with the set-up, running and close out of sites in a clinical trial.

JOB RESPONSIBILITIES:

Responsible for investigator site management and monitoring for assigned sites: Clinical Trial Monitoring

• Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan and applicable prevailing laws, Good Clinical Practices, and Pfizer standards to achieve project goals, timelines and quality

• Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site initiation through to database lock, ensuring relevant timelines and quality deliverables are met.During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery

• Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites

• Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks

• Attend investigator meetings when required (virtual or F2F).

• Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level

• Conduct remote assessment of e diary data

• Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the Study Monitoring Plan, SOPs and commensurate with emerging issues and technologies.

• Monitor site level AEs and SAEs and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution

• Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics

• Identify and resolve investigator site issues within required timeframes; agree and develop corrective and preventative actions with investigator and site personnel to close open issues and to prevent recurrence/persistence of issues

• Resolve data queries within required timelines, prepare investigator site close-out plan and conduct close-out activities within required timelines

• Ensures adequate oversight of the investigational product at the investigator site, including receipt, handling, accounting, storage conditions, and destruction activities.

• Support database release as needed

• May undertake the responsibilities of an unblinded monitor where appropriate.Clinical/Scientific and Site Monitoring Risk:

• Maintain thorough understanding of the product, protocol and therapy area in sufficient details to have appropriate discussions with the investigator and site team

• Interact with investigator site health care professionals in a manner which enhances Pfizer’s credibility, scientific leadership and in order to facilitate Pfizer’s clinical development goals

• Support the study clinician in ensuring patient safety, eligibility and providing clinical guidance to investigators

• Drive Quality Event submission and remediation, when applicable

• Serve as a point of contact for audit conduct, and drive Audit Observation CAPA development and checks, when applicable.

QUALIFICATIONS:

Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
Knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations
Monitoring Experience: Minimum 1-year relevant experience in clinical research site monitoring and management
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience preferred
Must be fluent in English and in the native language(s) of the country they will work in.

PHYSICAL/MENTAL REQUIREMENTS:

Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Demonstrated knowledge in disease and technical areas pertaining to clinical studies, including knowledge of company direction, investigational product(s), and associated development plan(s)
Demonstrated understanding of region/country, culture, and medical practice and how they affect clinical trial delivery
Ability to work in a matrix team environment with the ability to influence, drive / lead and work through others for successful delivery of clinical trial
Ability to evaluate, interpret and present complex issues and data to support risk management and mitigation
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS:

Significant travel (60-80%) within area is required. May require some international travel and some weekend travel.

ORGANIZATIONAL RELATIONSHIPS:

Partners with Site Care Partner and Country SOM
Reports to Director of Clinical Site Operations, or Director of Site Management and Monitoring, or Site Care Partner III in some countries
When required Partners with other Study Team members e.g. Clinician, Recruitment Specialist, Clinical Data Scientist

Work Location Assignment: Remote

Last date to apply for job: Oct 21st

EEO (Equal Employment Opportunity) & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

Medical

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Full time
Medical
Regular

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