Mumbai City, Maharashtra, India · Remote OK
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Performs aggregate medical revi…
Skills: Medical Safety, Signal Detection, Pharmacovigilance, Medical Review, Case Processing
Sydney, New South Wales, Australia · Hybrid
We’re excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaning…
Skills: Clinical Monitoring, ICH GCP Guidelines, Site Management, Source Data Verification, Regulatory Compliance
Madrid, Community of Madrid, Spain · Remote OK
Job Overview: The Director level of Clinical Delivery Center of Excellence (CoE) is an experienced leader within the Clinical Delivery CoE, they are expected to leverage their leadership competencies, clinical delivery e…
Skills: Clinical Delivery, Project Management, Financial Stewardship, Client Relationship Management, Risk Management
Budapest, Central Hungary, Hungary · Remote OK
Job Overview: The Director level of Clinical Delivery Center of Excellence (CoE) is an experienced leader within the Clinical Delivery CoE, they are expected to leverage their leadership competencies, clinical delivery e…
Skills: Clinical Delivery, Financial Stewardship, Project Management, Client Relationship Management, Risk Management
Bengaluru, Karnataka, India · On-site
Job Overview: The Senior Director, Strategic Accounts will serve as a strategic business partner responsible for leading complex sales efforts and developing, expanding, and deepening new business opportunities within as…
Skills: Strategic Account Management, Business Development, Consultative Selling, Commercial Strategy, Executive Presence
São Paulo, São Paulo, Brazil · On-site
Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Pro…
Skills: Site Monitoring, Site Management, Clinical Trial Management, Regulatory Compliance, Case Report Forms
Manila, Metro Manila, Philippines · Hybrid
Summary of Responsibilities: To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc.Receive information, record, and report Adver…
Skills: Medical Information Query Handling, Product Quality Complaint Management, Adverse Drug Reaction Reporting, Drug Safety Data Management, Call Intake
Bengaluru, Karnataka, India · Remote OK
Job Overview: We’re seeking a Workday Configuration Developer Manager to assist with design and end‑to‑end solutioning across our Workday PATT portfolio Summary of Responsibilities: Configure and maintain Workday Payroll…
Skills: Workday Configuration, Workday Payroll, Workday Absence, Workday Time Tracking, Solution Design
Beijing, Beijing, China · Hybrid
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including veri…
Skills: Clinical Monitoring, ICH GCP Guidelines, Site Management, Source Data Verification, eCRF Review
Mumbai City, Maharashtra, India · Remote OK
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical revie…
Skills: Medical Review, Pharmacovigilance, Case Processing, Signal Detection, ICH-GCP Guidelines
Istanbul, Istanbul, Turkey · Remote OK
We are currently seeking a Senior Associate Regulatory Submissions in Türkiye. In this role, you will be embedded within our Functional Service Provider (FSP) department, working closely with an international client in a…
Skills: Regulatory Submissions, Clinical Trial Authorizations, CTA/IND Processes, ICH-GCP, GMP
Leeds, England, United Kingdom · On-site
Fortrea's Clinical Research Unit in Leeds is where life-saving medicines begin their journey. You’ll be part of a team that asks one crucial question: will this new medicine be safe? If you enjoy working in a fast-paced …
Skills: Sample Processing, Laboratory Techniques, Data Documentation, Inventory Management, Hazardous Materials Handling
Warsaw, Masovian Voivodeship, Poland · Remote OK
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a …
Skills: Clinical Site Monitoring, Site Management, Source Document Review, SAE Reporting, CRF Review
Durham, California, United States · Remote OK
$200k–$220k/yr
Job Overview: The Sr. Director, Executive Compensation will own the strategy, design, and implementation of executive compensation programs, including base pay, short-term incentive programs, long-term incentive structur…
Skills: Executive Compensation Design, Equity Administration, Incentive Program Management, Financial Acumen, Stakeholder Management
Durham, California, United States · Remote OK
Our FSO team is seeking an Ophthalmology Senior Clinical Project Manager or Clinical Project Manager II to join our growing team. This role requires 3+ years of global project management experience, with mandatory experi…
Skills: Clinical Project Management, Ophthalmology, Budget Management, Risk Management, Stakeholder Management
Durham, California, United States · Remote OK
Our FSO team is seeking an Cell & Gene Therapy Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5+ years of global project management experience, with mandatory experience…
Skills: Clinical Project Management, Cell & Gene Therapy, Risk Management, Budget Management, Stakeholder Management
Sofia, Sofia-City, Bulgaria · Remote OK
Job Overview: Our FSO team is seeking an Ophthalmology Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3+ years of global project management experience, with mandatory exper…
Skills: Clinical Project Management, Ophthalmology, Budget Management, Risk Management, Stakeholder Management
Sofia, Sofia-City, Bulgaria · Remote OK
Job Overview: Our FSO team is seeking a General Medicine Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3+ years of global project management experience, with mandatory exp…
Skills: Clinical Project Management, General Medicine, Budget Management, Risk Management, Stakeholder Management
Sofia, Sofia-City, Bulgaria · Remote OK
Job Overview: Our FSO team is seeking an Oncology Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3+ years of global project management experience, with mandatory experience…
Skills: Clinical Project Management, Oncology, Budget Management, Risk Management, Stakeholder Management
Shanghai, Shanghai, China · Hybrid
This role is for upcoming future opportunities that may arise at Fortrea. Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interv…
Skills: Clinical Trial Administration, TMF Management, Project Tracking, Microsoft Office Suite, Document Control
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Provide medical safety expertise to sponsors of drugs and devices during the post-marketing period. Perform aggregate medical reviews, signal detection, and manage case data tracking to ensure compliance with SLAs and KPIs.
Requires a Bachelor's degree in medical science, MD, or DO, with working knowledge of medical sciences and ICH-GCP guidelines. Preferred candidates have up to 2 years of pharmaceutical industry experience in pharmacovigilance or clinical practice.
Job Overview:
Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period.
Summary of Responsibilities:
Qualifications (Minimum Required):
Experience (Minimum Required):
Preferred Qualifications Include:
Physical Demands/Work Environment:
Learn more about our EEO & Accommodations request here.
Bringing life-changing benefits to patients faster
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators. Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas. Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes. Together, exceptional is possible. Learn more at Fortrea.com
Offices: Research Triangle Park, NC, US
Bringing life-changing benefits to patients faster
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators. Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas. Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes. Together, exceptional is possible. Learn more at Fortrea.com
Offices: Research Triangle Park, NC, US
