In-House Clinical Research Associate — TMF & Regulatory
$50k - $80kTechnical Resources International Inc
Technical Resources International, Inc. in Bethesda, MD is seeking an In-House Clinical Research Associate to support clinical study teams with regulatory document management and compliance tasks. The ideal candidate holds a Bachelor's Degree and possesses excellent negotiation, communication, and organizational skills. The role demands proficiency in Microsoft Office and may involve regulatory document review experience. The salary range is $50,000-$80,000 annually, with no travel required. #J-18808-Ljbffr Technical Resources International, Inc.
$50k - $80k
Piper Companies is seeking an In-House Clinical Research Associate located in Bethesda, MD. The role involves reviewing and processing regulatory documents, maintaining Trial Master Files, and ensuring compliance with FDA and ICH GCP guidelines. Ideal candidates will have...HouseRegulatory$50k - $80k
...Piper Companies is looking for an In-House Clinical Research Associate to join a clinical research company... ...Responsibilities Review and process essential regulatory documents received from clinical... ...and organize Trial Master Files (TMF) and centralized document systems...HouseRegulatoryWork at office- ...In-House Clinical Research Associate - (IHCRA001_COMPANY_1.1) Job Title: In-House Clinical Research Associate Location... ...Retrieve, file, and maintain essential regulatory documents from clinical trial sites for the Trial Master File (TMF) or another central documents file...HouseRegulatoryFull timeWork at officeLocal area
$70k - $110k
...Clinical Research Associate The Clinical Research Associate (CRA) is primarily... ...guidelines, local and global regulatory requirements, and Novotech/... ...collaboration with the In-house Clinical Research Associate... ...project Trial Master File (TMF) is up to date, current and...HouseRegulatoryContract workLocal areaRemote workFlexible hours$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Washington DC ICON plc is a world... ...document collection and TMF reconciliation with site files... ...sites and the client's regulatory inspections Contribute to... ...Functional Services (or in-house) monitoring model is preferred...HouseRegulatoryInterim roleLocal areaRemote workFlexible hours$50k - $70k
Piper Companies is seeking a Clinical Research Associate (CRA) to support the operational delivery of... ...study teams, driving site performance, regulatory compliance, and data quality. This... ...experience (CRO, sponsor, or site), in-house preferred. Prior experience in in-house...HouseRegulatoryRemote work$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Washington DC ICON is a global... ...essential document collection and TMF reconciliation with site... ...sites and the client's regulatory inspections Contribute to... ...Functional Services (or in-house) monitoring model is preferred...HouseRegulatoryInterim roleLocal areaRemote work- ...In-House Clinical Research Associate The In-House Clinical Research Associate (CRA) is responsible for assisting with operational activities supporting... ...in accordance with the protocol, SOPs, and applicable regulatory requirements. The role may also be referred to as a...HouseRegulatoryInterim roleRemote work
- ...being are protected Collects, reviews, and monitors required regulatory documents for study start-up, study maintenance, and study... ...and escalates per protocol to upper management Work with in-house Clinical Trial Assistant to collect, review, and monitor required...HouseRegulatoryInterim roleLocal areaRemote workFlexible hours
- Emmes Group is seeking an In-House Clinical Research Associate to support operational activities for clinical trials. The role involves assisting... ...trial progress and ensuring compliance with protocols and regulatory standards. The ideal candidate will have a Bachelor's...HouseRegulatory
$120k - $140k
Sr. Oncology Clinical Research Associate $120000 - $140000 per year | Germantown, MD | Remote | Permanent... ..., reviews, and monitors required regulatory documents for study start-up, study maintenance... ...to upper management Work with in-house Clinical Trial Assistant to collect,...HouseRegulatoryPermanent employmentInterim roleLocal areaRemote workFlexible hours- ...Clinical Research Associate – Full-Service Syneos Health is a fully integrated biopharmaceutical solutions... ...on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiology... ...it with the Trial Master File (TMF), and ensure sites are aware of archiving...RegulatoryInterim roleLocal areaImmediate startRemote workFlexible hours
- ...Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is a leading fully integrated... ...on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiology... ...the ISF with the Trial Master File (TMF). Ensures the investigator/physician...RegulatoryContract workInterim roleLocal areaImmediate startRemote workFlexible hours
$101.6k - $169.3k
...IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular... ...of assigned studies by tracking regulatory submissions and approvals, recruitment... ...for filing in the Trial Master File (TMF) and verify that the Investigator's Site...RegulatoryFull timePart timeLocal areaImmediate startWorldwide- ...full-service Contract Research Organization (CRO) supporting... ...With expertise across Clinical Operations, Biometrics... ...Pharmacovigilance and Regulatory Affairs, we partner... ...Clinical Research Associates (CRAs) to support future... ...Trial Master File (TMF) management Site training...RegulatoryContract workWorldwide
$47.59k - $87.56k
...Responsibilities The candidate will provide clinical and research services to clinical trial subjects... ...situations. The Clinical Research Associate works directly with clinical trial... ...teams to ensure objectives are met and regulatory compliance is maintained Collaborates...RegulatoryWork experience placementWork at office- Overview Clinical Research Associate II US Remote Emmes Group: Building a better future for us all. Emmes Group is transforming... ...operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. The CRA will conduct monitoring visits and...RegulatoryWork experience placementInterim roleCasual workLocal areaRemote workWork from homeFlexible hours
- ...Emmes in Rockville, Maryland is searching for an In-House Clinical Research Associate to help advance global health through innovative clinical research. You will play a key role in managing essential trial documentation, assisting with site communications, and ensuring...House
- ...therapy experience is strongly preferred. Job Purpose: The Clinical Research Associate (CRA) has local responsibility for the delivery of the... ...as required, CRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits,...RegulatoryLocal areaRemote workFlexible hoursShift work
- ...Position: Senior Clinical Research Associate (level dependent on experience) Location: Washington, DC Job Id: CRA ongoing WA # of Openings... ...form (CRF) retrieval / source document review (SCV), regulatory documents, and investigational product. Participates...RegulatoryLocal areaRemote workWork from homeHome office
$73.6k - $85k
...Clinical Research Associate Responsible for assessing the study capabilities of potential study sites, training, on-site monitoring, closure... ...Forms, and resolving all data queries Review the regulatory binder and essential documents at the site and verify all...RegulatoryFull timeWork experience placementInterim roleWork at officeLocal areaRemote workNight shift- ...Job Summary The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is... ...required, SrCRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits,...RegulatoryLocal areaRemote workFlexible hoursShift work
$40k - $50k
A clinical research organization is seeking a TMF Specialist in Bethesda, MD, for a hybrid role with three remote days weekly. The successful candidate will manage TMF set-up, document quality, and regulatory compliance. Applicants should have at least one year of TMF...RegulatoryRemote job- ...support the financial operations of a portfolio of affordable housing communities. This role is ideal for a detail-oriented accounting... ...HUD REAC submissions and ensure compliance with state and regulatory reporting requirements Coordinate with lenders and investors to...HouseRegulatoryFull time
- ...engineering, manufacturing and field services by providing commercial and technical product regulatory expertise related to low and medium voltage power distribution equipment, E-houses and control systems. This role will support the entire regulatory process with NRTLs,...HouseRegulatoryWork at office
- Join Emmes as an In-House Clinical Research Associate, where you'll assist in monitoring clinical trials to ensure compliance with regulations. The role requires a Bachelor's degree in a scientific discipline and involves coordinating with both project and site staff to...House
- Syneos Health/ inVentiv Health Commercial LLC is looking for an Experienced Clinical Research Associate to ensure regulatory compliance and performance at clinical sites. Responsibilities include site monitoring, documentation, and supporting subject recruitment strategies...RegulatoryRemote job
$40k - $50k
Overview Piper Companies is looking for a TMF Specialist to join a clinical research organization (CRO). This is a hybrid position with 3 remote days out... ...with eTMF specifications, ICH/GCP guidelines, regulatory requirements, and applicable SOPs. Ensures that all new...RegulatoryRemote work3 days per week- Emmes is seeking an In-House Clinical Research Associate who will be responsible for supporting project teams and ensuring compliance with regulations. This role includes tracking trial progress, maintaining essential documents, and communicating with site staff. The ideal...House
- ...involves collaboration with cross‑functional clinical study teams and investigator site... ..., monitoring plan, ICH GCP, local regulatory requirements, and client SOPs. Conduct... ...of study metrics, assess CRO Clinical Research Associate (CRA) and Investigator Site performance...RegulatoryInterim roleLocal areaRemote work
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