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, Blood Draws, ECG, Phlebotomy, Clinical Research Protocols
Buenos Aires, Argentina · Remote OK
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
Shanghai, Shanghai, 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: Site Monitoring, ICH GCP Guidelines, Source Data Verification, Clinical Trial Management, eCRF Review
Shanghai, Shanghai, China · Remote OK
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 · On-site
Summary of Responsibilities: To complete Other duties/activities as assigned by study management team, but not limited to:Manage clinical systems and access management.Maintain study databases (CTMS, IWRS, EDC, etc.)Supp…
Skills: Clinical Trial Management Systems, eTMF Management, Data Review, ICH-GCP Guidelines, Investigator Payments
Leeds, England, United Kingdom · On-site
What if your clinical operations expertise helped new medicines take their first step in human clinical trials? Fortrea is one of the largest and longest‑established early‑stage clinical research organizations in the wor…
Skills: Clinical Trial Coordination, Study Set-up, Protocol Execution, GCP, ICH Guidelines
Durham, California, United States · Remote OK
$105k–$145k/yr
We are currently seeking Experienced Oncology CRAs to lead and support our Full Service Outsourcing team working with various sponsors. 1+ year of independent CRO/sponsor monitoring required. CAR-T desired. Open to major…
Skills: Clinical Monitoring, Site Management, Oncology, CAR-T, Case Report Forms
Bengaluru, Karnataka, India · On-site
Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing …
Skills: Pharmacovigilance, Project Management, Adverse Event Reporting, MedDRA Coding, Regulatory Compliance
Shanghai, Shanghai, 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: Site Monitoring, ICH GCP Guidelines, Source Data Verification, Clinical Trial Management, eCRF Review
Durham, California, United States · Remote OK
$125k–$140k/yr
Our FSP team is currently seeking Sr. CRA 2s with 4+ years of monitoring residing in the East Coast, Midwest & West Coast US! WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a …
Skills: Clinical Monitoring, Site Management, Case Report Forms (CRF), Serious Adverse Event (SAE) Reporting, Registry Management
Milan, Lombardy, Italy · Remote OK
$32k–$488k/yr
Job Overview: Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required.…
Skills: Site Management, Regulatory Compliance, ICH/GCP Guidelines, Contract Negotiation, Budget Negotiation
Dallas, Texas, 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 CRF Specialist, to be responsible for transcribing and man…
Skills: Data Transcription, Case Report Forms, Clinical Research, Quality Control, Project Management
County Laois, The Municipal District of Graiguecullen — Portarlington, Ireland · Remote Solely
We are currently seeking a RWE Database Analyst Programmer to join a sponsor-dedicated team supporting a global pharmaceutical partner. This is a fully home-based opportunity located in either Poland or the United Kingdo…
Skills: RWE Data Analytics, SAS Programming, R Programming, Python Programming, Epidemiology
Bengaluru, Karnataka, India · Remote OK
Role Overview The Workday Security Lead/Senior Manager is responsible for driving the design, governance, and continuous enhancement of the Workday security framework across the enterprise. This role ensures secure, scal…
Skills: Workday Security, Security Architecture, Governance, Access Control Management, SOX Compliance
Daytona Beach, Florida, United States · On-site
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: Venipuncture, Blood Pressure Monitoring, ECG/Holter Recording, Biological Sample Processing, Clinical Research Protocols
Mumbai City, Maharashtra, India · Hybrid
Job Overview: Responsible for the preparation and review of aggregate safety, risk management, and signal detection documents. Perform report management activities and lead client communication for the assigned reports. …
Skills: Medical Writing, Pharmacovigilance, Signal Detection, Regulatory Submissions, Literature Search
Durham, California, United States · Hybrid
$230k–$275k/yr
The Executive Director, HR and Workday Platform Technology is the primary technology platform leader for Human Resources and Facilities and the enterprise platform owner for Workday. This role is accountable for the stra…
Skills: Workday HCM, Enterprise Application Leadership, Strategic Planning, Platform Governance, Product Management
Guangzhou City, Guangdong Province, China · On-site
Job Overview: Collaborate with peers across the organization to achieve client-centric delivery in a matrix organization. Collaboration across all stakeholders within Site Readiness. Oversight and accountability of Regul…
Skills: Regulatory Submissions, Submission Strategy, Project Management, Compliance, Quality Control
Leeds, England, United Kingdom · On-site
Fortrea is looking for an HR Advisor to join our Leeds team Full time, permanent, hybrid working The HR Advisor is an amazing opportunity to step into the clinical industry in a hands-on role where you will be at the hea…
Skills: Employee Relations, Performance Management, HR Analytics, Employment Law, Policy Compliance
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
Dallas, Texas, United States • On-site
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Provide high-standard clinical care for healthy volunteers in early phase clinical trials. Responsibilities include screening participants, obtaining informed consent, and performing protocol-required assessments.
Requires a high school diploma or equivalent, with a preference for EMT, Phlebotomy, CMA, or CNA certifications. Candidates must have experience taking vitals, performing blood draws, and conducting ECGs.
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 Units in the UK and US.
We are currently seeking a OPV (Outpatient Visit) Research Technician, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.).
This is a PRN, on‑site position in Dallas, TX, with hours based on study needs, including early mornings, extended hours, and weekends.
If you join us, you will work with some of the world´s leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.
Many are drawn to their profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know you´ll touch many patient´s lives around the world.
WHAT YOU WILL DO:
You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care clinical research.
Other key responsibilities:
Review study protocols and eligibility criteria to support participant screening.
Coordinate special screening procedures with study and recruitment teams.
Assist with development and accuracy of participant eligibility questionnaires.
Prepare and organize screening, consent, medical history, and study documentation.
Obtain informed consent and collect medical histories from participants.
Perform and/or coordinate protocol-required screening procedures and assessments.
Review screening records for accuracy, completeness, and compliance.
Prepare screening charts for physician and study manager review.
Maintain accurate participant status records within the study database.
Other duties as assigned.
High school diploma or equivalent
1-2 years research experience may be substituted for education requirement.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
EMT, Phlebotomy, CMA or CNA certification, preferred.
Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.
Occasional drives to site locations, occasional domestic travel.
Exposure to biological fluids.
Personal protective equipment required such as protective eyewear, garments, and gloves.
Ability to work in an upright and /or stationary position for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Regular and consistent attendance.
Varied hours may be required.
The important thing for us is you are comfortable working in an environment that is:
Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
Changing priorities constantly asking you to prioritize and adapt on the spot.
Teamwork and people skills are essential for the study to run smoothly.
Technology based. We collect our data directly into an electronic environment.
Regular, full-time, or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
401(K)
Paid time off (PTO)
Employee recognition awards
Multiple ERG’s (employee resource groups)
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
