Clinical Research Job at Fortrea, USA | Life Sciences | Apply Now
If you are an early-career clinical operations professional or administrative specialist looking to establish your career within a world-class global Contract Research Organization (CRO), this position is an exceptional opportunity. Based out of Durham, North Carolina, and offering a fully remote framework within the United States, this role embeds you directly into active multi-center clinical trials. For detail-oriented coordinators searching for a high-impact Clinical Research Job, this position offers hands-on ownership of Trial Master File (TMF) quality control, investigator site file maintenance, and clinical logistics tracking. It serves as an elite operational launchpad for a long-term Fortrea career (formerly part of Labcorp) and stands out as a premier choice for anyone tracking a foundational Life Sciences Job within a stable Functional Service Provider (FSP) model.
- Job Position: Clinical Trials Associate I
- Location: Durham, USA
- Job Requisition ID: 263295
About The Company
Fortrea is a leading global Contract Research Organization (CRO) driven by a unified mission to bring life-changing therapies to patients faster. Spun off as an independent powerhouse from Labcorp’s clinical development engine, Fortrea manages robust clinical development pipelines spanning biostatistics, patient recruitment, and multi-phase trial logistics for global pharmaceutical and biotechnology innovators.
Operating under a Functional Service Provider (FSP) team model, you will be dedicated directly to a single global pharmaceutical sponsor. This structure gives you the unique advantage of mastering the sponsor’s specific technology platforms, standard operating procedures (SOPs), and clinical trial management systems (CTMS), while maintaining the robust career trajectory, training programs, and employment stability of an international CRO.
Clinical Research Job – Key Responsibilities
As a Clinical Trials Associate I (also functioning as a Clinical Trial Administrator), you will act as a core operational engine of the Clinical Project Team, ensuring all study metrics and regulatory logs remain in total compliance with strict protocols.
Your primary tracking, administrative, and clinical support duties include:
- TMF Governance & Quality Control: Uploading and archiving regulatory documents within the central electronic Trial Master File (eTMF) platform, participating in systematic TMF QC audits, and flagging missing or expired records.
- Investigator File Coordination: Setting up, updating, and maintaining clinical investigator files and site documentation pre- and post-Site Initiation Visits (SIV).
- Supply & Shipment Logistics: Coordinating with external vendors to plan, package, and ship critical study supplies to investigative clinics. You will verify shipment manifests and track courier data (tracking numbers, delivery confirmations) for notebooks, case report forms (CRFs), and patient diaries.
- CTMS Data Reconciliation: Generating automated reporting vectors—such as site contact lists—and partnering with In-House Clinical Research Associates (CRAs) to perform data reconciliation inside the Clinical Trial Management System (CTMS) to advance this Clinical Research Job.
- Meeting & Minutes Management: Documenting and tracking project milestones across relevant internal and sponsor-facing systems, including drafting official minutes for project teleconferences and tracking Investigator Meeting attendees.
- Vendor & Access Management: Liaising with third-party vendors for material printing and securing external systems access and digital credentials for regional trial staff to support this Life Sciences Job.
Qualifications & Profile Requirements For Clinical Research Job
This entry-to-junior operational role is meticulously designed for high-dexterity, detail-driven professionals who can thrive in a highly regulated, technology-based environment where protocol deviations are not permitted.
- Required Criteria:
- Educational Foundation: A formal Bachelor’s degree in a life sciences or related quantitative discipline. Alternatively, an Associate’s degree in a life sciences field paired with a minimum of 2 years of directly relevant industry experience will be accepted.
- Administrative Baseline: A minimum of one (1) year of administrative experience or equivalent corporate training to secure a baseline trajectory for your Fortrea career.
- Regulatory Compliance Grounding: A general, conceptual knowledge of international clinical research principles, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Legal Authorization: Full, permanent authorization to work in the United States indefinitely without requiring current or future corporate visa sponsorship. Residing within the US is mandatory.
- Technical Skills & Competencies:
- Strong computer literacy across the Microsoft Office Suite (Word, Excel, PowerPoint), with an aptitude for editing spreadsheet calculations and numerical data.
- Sharp typing, spelling, and proofreading skills to handle precise sponsor communications.
- Ability to work effectively within a fast-paced matrix environment characterized by rapidly shifting priorities and hard timeline closures.
Logistics, Physical Demands & Target Compensation
- Location: Durham, NC / Fully Remote (#LI-Remote) within the United States.
- Employment Type: Regular, Full-Time.
- Job Requisition ID: 263295.
- Target Salary Range: $45,000.00 – $50,000.00 USD Annually (Actual baseline salary depends on budget, prior administrative exposure, and localized skillsets).
- Physical & Agility Demands: Prolonged periods of sitting and computer operation; repetitive finger, hand, and wrist movements; occasional bending, twisting, crouching, or stooping; ability to lift and carry up to 15–20 lbs (such as laptops and boxed study supplies).
In short, the Clinical Trials Associate I position is a definitive route to transitioning your science degree or administrative background into a highly marketable, international clinical operations asset. Securing this appointment allows you to move past generalized clerical duties and take direct operational charge of the eTMF quality workflows, vendor supply streams, and CTMS tracking systems that steer multi-million dollar pharmaceutical assets through global clinical pipelines. If you reside in the United States, meet the 1-year administrative threshold, and possess an absolute zero-deviation mindset for data quality, apply today to secure this premier Clinical Research Job, launch a highly rewarding Fortrea career, and lock in this outstanding Life Sciences Job.
