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- ...Clinical Research Associate Our client, a leading organization in the clinical... ...is seeking a dedicated In-House Clinical Research Associate... ...Review and process essential regulatory documents received from clinical... ...Trial Master Files (TMF) and centralized document systems...HouseRegulatoryWeekly payTemporary workFlexible hours
- ...Job Title In-House Clinical Research Associate Location Bethesda, MD 20817 US (Primary) Category... ...Retrieve, file, and maintain essential regulatory documents from clinical trial sites for the Trial Master File (TMF) or another central documents file platform...HouseRegulatoryFull timeWork at officeLocal areaRemote work
$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$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... ...Functional Services (or in-house) monitoring model is...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- ...Overview Clinical Research Associate I Be Part of One Team, One Purpose. At Emmes Group, we’... ...(SOPs), ICH GCP, and all applicable regulatory requirements. The CRA will conduct monitoring... ...research experience (as a CTA, in-house CRA, CRC etc.) preferred Preferred...HouseRegulatoryWork experience placementInterim roleCasual workLocal areaRemote workWork from homeFlexible hours
- ...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
- ...Tenacity Solutions, LLC (Tenacity) is seeking an experienced Clinical Research Quality Associate (CRQA) to support the Department of Veterans Affairs (... ...protocol compliance, review informed consent and regulatory documentation, verify source data, identify compliance...RegulatoryContract workWork at officeImmediate startRemote work
- ManpowerGroup Global, Inc. is seeking an In-House Clinical Research Associate in Bethesda, MD to support clinical operations. The role emphasizes regulatory document review, TMF management, and ensuring FDA/ICH GCP compliance. You will coordinate documentation, maintain...HouseRegulatory
- 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
- ...Job Description Job Description The House Supervisor maintains nursing unit goal and objectivea and is responsible for the supervision... ...with company policy as well as federal, state, and local regulatory requirements. The House Supervisor coordinates programs and services...HouseRegulatoryLocal areaShift workWeekend work
- Harbor Group Management Company is seeking a Multifamily Compliance Specialist to ensure regulatory compliance across properties participating in affordable housing programs (LIHTC, HOME, HUD, Section 8). The role collaborates with Regional Managers, Operations, and Compliance...HouseRegulatory
$44.02k - $73.41k
...Requirements Job Overview The Clinical Research Coordinator I (CRCI) is responsible for... ...requirements include, but are not limited to: Regulatory maintenance, Adherence with ongoing... ...basis, the CRC I will report to the Associate Director of Clinical Trials. The CRC I...RegulatoryHourly payFull timeWork experience placementWork at office- ...Job Purpose: The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active... ...as required, CRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits,...RegulatoryLocal areaRemote workFlexible hoursShift work
- ...Overview We are seeking a motivated and detail-oriented Clinical Research Assistant to join our growing clinical operations team. In this... ...while ensuring study documentation, data quality, and regulatory compliance are maintained throughout the research process....RegulatoryFull timeWork at officeRemote workMonday to Friday
$160k - $180k
...governance and compliance matters, with a focus on energy sector regulatory requirements and internal policies. This is a dynamic position... ...of legal experience, with at least 3 years at a law firm or in‑house legal department focused on commercial transactions, project...HouseRegulatoryFull timeContract workLocal area$83k - $114.2k
...As the Clinical Research Associate II, you will be responsible for planning, execution and oversight of clinical studies in compliance with ICH-GCP and IVD clinical guidelines, applicable regulatory requirements, and company SOPs. This role participates in the management...RegulatoryFull timeWork experience placementWork at office$47.59k - $87.56k
...Overview The candidate will provide clinical and research services to clinical trial subjects... ...clinical situations. The Clinical Research Associate works directly with clinical trial... ...to ensure objectives are met and regulatory compliance is maintained Collaborates...RegulatoryHourly payFull timeWork experience placementWork at office- ...financial operations and monthly reporting for a portfolio of housing properties. This role offers the opportunity to work within a... ...environment involving housing subsidies, compliance reporting, and regulatory escrows. Key Responsibilities Prepare monthly...HouseRegulatory
- Emmes Group in Rockville, Maryland is seeking a Senior Clinical Research Associate to oversee monitoring of clinical study sites, ensuring compliance with regulatory requirements and protocols. This role involves conducting both remote and on-site visits, documenting findings...RegulatoryRemote work
- Victory Housing, Inc. is seeking an experienced Health, Wellness and Clinical Program lead to oversee nursing assessments, care planning and quality assurance for all... .... The position emphasizes staff mentorship, regulatory compliance, and collaborative care planning with...HouseRegulatory
- ...DoExpert in the field of drug research and development,... ...guide the full lifecycle of clinical research and development projects... ...spanning research, development, regulatory, marketing, and manufacturing... ...stakeholders. • Manage activities associated with audits to ensure...RegulatoryFull timeLocal area
$96k - $107k
...maintaining, and updating the Xometry legal and regulatory compliance programs. This role will work... ...teams and functions Performing legal research Electronically maintaining and... ...Dependable, reliable and a strong work ethic In‑house, public company experience a plus...HouseRegulatoryWork experience placementLocal area$230k - $300k
...structuring and launch through ongoing disclosure, reporting, and regulatory engagement—with high visibility, real accountability, and less... ...asset management industry (law firm and/or sophisticated in-house environment).Deep knowledge of the Securities Act of 1933 and Securities...HouseRegulatory- Description Clinical Research Associate Venesco LLC is seeking a Clinical Research Associate (CRA) to provide clinical monitoring and oversight... ...protocol compliance and identify deviations. Review regulatory binders and essential documents. Generate clinical monitoring...Regulatory
- ...Responsibilities Ensure that the attainment of Victory Housing mission takes precedence over all decisions and actions. Oversight... ...of food service and supervision of dietary staff. Meet all regulatory requirements and maintains quality food service within budget....HouseRegulatory
- ...Clinical Research Coordinator Live and work in a thriving urban center near the nation's capital... ...a local church, the Bethesda Meeting House (1820, rebuilt 1849), which in turn... ...protocols, is ethically-conducted and follows regulatory standards Maintaining research...HouseRegulatoryLocal area
- Emmes Group in Rockville, MD is seeking a Clinical Research Associate I to monitor clinical study sites, conduct site visits, and ensure trials comply with protocol, SOPs, ICH GCP, and regulatory requirements. You will perform site visits, informed consent reviews, source...RegulatoryRemote job
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