Milan, Lombardy, Italy · On-site
$48k–$63k/yr
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, Regulatory Compliance, Clinical Trial Management, Case Report Forms Review
Mumbai City, Maharashtra, India · On-site
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the postmarketing period; and may manage a team. Summary of Responsibilities: Undertake…
Skills: Medical Review, Pharmacovigilance, Case Processing, Signal Detection, Aggregate Safety Reports
Bengaluru, Karnataka, India · Hybrid
Job Overview: The Associate Medical Data Review Manager is an important member of the Global Medical Review Team with responsibility for execution of key Central Medical Review activities within the Central Monitoring st…
Skills: Central Medical Review, Central Monitoring, Medical Data Review, Signal Detection, Risk Assessment
Manila, Metro Manila, Philippines · Hybrid
Job Overview: Analyze training needs in collaboration with subject matter experts and relevant stakeholders. Delivers and implements training for employees with learning principles and appropriate standard operating proc…
Skills: Training Needs Analysis, Curriculum Development, Pharmacovigilance Regulations, Medical Information Synthesis, Microsoft Office Suite
Guangzhou City, Guangdong Province, 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
Guangzhou City, Guangdong Province, China · On-site
Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. T…
Skills: Site Monitoring, Site Management, Clinical Research, Regulatory Compliance, Case Report Forms
Bengaluru, Karnataka, India · Hybrid
Summary of Responsibilities: • Ensures that all allocated projects are carried out in strict accordance with the relevant protocols, global harmonized SOPs, and the specified standards of GCPs. • Demonstrates capability …
Skills: Clinical Data Management, GCP, SOPs, Data Review, Query Management
pune, Maharashtra, India · Remote OK
Job Overview: To coordinate with Finance and Delivery team to facilitate the data requirement of Projected and Rolled up Revenue, Project level Margin, Raising Invoicing, Preparing Account/Project level business review d…
Skills: Financial Processes, Microsoft Excel, Data Aggregation, Macro Development, Project Cost Allocation
Guangzhou City, Guangdong Province, China · On-site
Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project …
Skills: Site Monitoring, Site Management, Clinical Trial Process, Regulatory Guidelines, ICH GCP
Durham, California, United States · Remote OK
$125k–$140k/yr
Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5+ years of monitoring residing in the NYC Metro or PHL area. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a hig…
Skills: Clinical Monitoring, Oncology, Site Management, Case Report Forms, SAE Reporting
Herzliya, Tel-Aviv District, Israel · On-site
The Senior Clinical Trial Administrator is a key member of the Clinical Project Team, supporting the delivery of clinical research projects. This role focuses on coordinating study activities, maintaining high-quality do…
Skills: Clinical Trial Coordination, Trial Master File (TMF) Management, Quality Control, Regulatory Compliance, Project Tracking
Maidenhead, England, United Kingdom · Remote OK
Job Overview: In this role, you’ll drive revenue growth across strategic and complex accounts through proactive outreach, smart networking, and sharp commercial execution. You’ll be the person who connects the dots—culti…
Skills: Business Development, Account Management, Strategic Planning, Negotiation, Pipeline Forecasting
Bengaluru, Karnataka, India · Hybrid
Summary of Responsibilities: To complete other duties/activities as assigned by study management team, but not limited to:Manage clinical systems and access management.Manage study documents and support eTMF management.M…
Skills: Clinical Systems Management, eTMF Management, CTMS, IWRS, EDC
Maidenhead, England, United Kingdom · Remote OK
Job Overview: The Designer liaises with consultancy teams and developers to create design concepts for interactive content (e.g., data display, presentation, or eLearning) that meet the client’s requirements and comply w…
Skills: Graphic Design, Interaction Design, UI Design, Adobe Creative Cloud, Photoshop
Leeds, England, United Kingdom · Remote OK
Job Overview: The Senior Director, Commercial and Marketing Technology Platforms plays a pivotal role in shaping and delivering Fortrea’s commercial and marketing technology ecosystem. This leader is responsible for the …
Skills: CRM Management, Marketing Technology Strategy, Product Management, Agile Methodologies, Budgeting
Durham, California, United States · Hybrid
$75k–$90k/yr
Job Overview The HR Business Analyst, Special Projects is responsible for supporting and leading strategic HR initiatives, projects, and process improvements that enhance organizational effectiveness and operational effi…
Skills: Project Management, HR Analytics, Stakeholder Management, Process Optimization, Change Management
São Paulo, São Paulo, Brazil · Remote Solely
Are you passionate about clinical trial budgeting, financial strategy, and delivering accurate, competitive study cost estimates? Join Fortrea as an Investigator Grants Manager / Clinical Trial Costing Manager and play a…
Skills: Clinical Trial Budgeting, Financial Analysis, Grants Management, Investigator Grant Estimates, Costing Strategies
Madison, Wisconsin, United States · On-site
As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a Dietary Coordinator to interact directly with our healthy …
Skills: Menu Creation, Nutritional Guidance, Inventory Management, Vendor Coordination, Data Entry
Durham, California, United States · Remote OK
$105k–$117k/yr
We are currently seeking Experienced Ophthalmology & Gen Med CRA 2s to lead and support our Full Service Outsourcing team. Open to major hub locations on the East & West Coast. 60-70% travel, 8-10 DOS per month. WHAT YOU…
Skills: Clinical Monitoring, Site Management, Case Report Forms, SAE Reporting, Patient Protection
Dallas, Texas, United States · On-site
*** Please note that this role requires you have experience with taking vitals, blood draws and ECG's.*** As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Uni…
Skills: Vitals Measurement, Blood Draws, ECG Performance, Clinical Research Protocols, Participant Screening
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The Sr CRA II is responsible for site monitoring, management, and ensuring regulatory compliance for clinical studies. This includes conducting site visits, verifying data integrity, and potentially serving as a Local Project Coordinator or Lead CRA.
Requires a university degree in a related health profession or 6 years of clinical monitoring experience, plus 3-4 years of specific monitoring experience. Candidates must have thorough knowledge of regulatory requirements and the drug development process.
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 Procedures, and Regulatory Guidelines. The Sr CRA II assures the implementation of project plans as assigned, functions as leader for projects of limited scope, as assigned and assumes line management responsibilities, as assigned. Acts in the project role of a Local Project Coordinator or Lead CRA as assigned.
Summary of Responsibilities:
Qualifications (Minimum Required):
Experience (Minimum Required):
Preferred Qualifications Include:
Physical Demands/Work Environment:
The base salary range for this role is € 47,800 - 63,000 gross per year, which may vary as per working schedule (full or part-time). The final offer will be determined based on objective and job-related criteria such as experience, qualifications, and scope of responsibilities, in line with our internal job classification framework and the applicable collective labour agreement (CCNL). This role may also be eligible for additional compensation, such as bonus and benefits, in accordance with company policies
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
