Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

In-House Clinical Research Associate — TMF & Regulatory

$50k - $80k

Technical 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.

Vacancy posted 5 days ago
Similar jobs that could be interesting for youBased on the In-House Clinical Research Associate — TMF & Regulatory in Bethesda, MD vacancy
  • $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... 
    House
    Regulatory

    Piper Companies

    Bethesda, MD
    6 days ago
  • $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... 
    House
    Regulatory
    Work at office

    Piper Companies

    Bethesda, MD
    2 days ago
  •  ...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... 
    House
    Regulatory
    Full time
    Work at office
    Local area

    Technical Resources International

    Bethesda, MD
    2 days ago
  • $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... 
    House
    Regulatory
    Contract work
    Local area
    Remote work
    Flexible hours

    Novotech

    Washington DC
    4 days ago
  • $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... 
    House
    Regulatory
    Interim role
    Local area
    Remote work
    Flexible hours

    ICON Clinical Research

    Washington DC
    1 day ago
  • $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... 
    House
    Regulatory
    Remote work

    Piper Companies

    Bethesda, MD
    5 days ago
  • $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... 
    House
    Regulatory
    Interim role
    Local area
    Remote work

    ICON

    Washington DC
    6 days ago
  •  ...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... 
    House
    Regulatory
    Interim role
    Remote work

    Emmes Group

    Rockville, MD
    3 days ago
  •  ...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... 
    House
    Regulatory
    Interim role
    Local area
    Remote work
    Flexible hours

    Jobot

    Washington DC
    1 day ago
  • 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... 
    House
    Regulatory

    Emmes Group

    Rockville, MD
    4 days ago
  • $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,... 
    House
    Regulatory
    Permanent employment
    Interim role
    Local area
    Remote work
    Flexible hours

    Australia-Employment

    Washington DC
    2 days ago
  •  ...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... 
    Regulatory
    Interim role
    Local area
    Immediate start
    Remote work
    Flexible hours

    Syneos Health/ inVentiv Health Commercial LLC

    Washington DC
    1 day ago
  •  ...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... 
    Regulatory
    Contract work
    Interim role
    Local area
    Immediate start
    Remote work
    Flexible hours

    Syneos Health/ inVentiv Health Commercial LLC

    Washington DC
    5 days ago
  • $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... 
    Regulatory
    Full time
    Part time
    Local area
    Immediate start
    Worldwide

    IQVIA

    Rockville, MD
    1 day ago
  •  ...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... 
    Regulatory
    Contract work
    Worldwide

    OPIS srl

    Washington DC
    6 days ago
  • $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... 
    Regulatory
    Work experience placement
    Work at office

    Georgetown University in Qatar

    Washington DC
    2 days ago
  • 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... 
    Regulatory
    Work experience placement
    Interim role
    Casual work
    Local area
    Remote work
    Work from home
    Flexible hours

    The Emmes Company, LLC

    Rockville, MD
    2 days ago
  •  ...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

    EMMES Corporation

    Rockville, MD
    3 days ago
  •  ...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,... 
    Regulatory
    Local area
    Remote work
    Flexible hours
    Shift work

    PAREXEL

    Washington DC
    5 days ago
  •  ...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... 
    Regulatory
    Local area
    Remote work
    Work from home
    Home office

    CTI Clinical Trial Services

    Washington DC
    4 days ago
  • $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... 
    Regulatory
    Full time
    Work experience placement
    Interim role
    Work at office
    Local area
    Remote work
    Night shift

    Glaukos Corporation

    Washington DC
    5 days ago
  •  ...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,... 
    Regulatory
    Local area
    Remote work
    Flexible hours
    Shift work

    PAREXEL

    Washington DC
    4 days ago
  • $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... 
    Regulatory
    Remote job

    Piper Companies

    Bethesda, MD
    4 days ago
  •  ...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... 
    House
    Regulatory
    Full time

    HRB

    Bethesda, MD
    1 day ago
  •  ...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,... 
    House
    Regulatory
    Work at office

    PwrQ Holdings LLC

    Garrett Park, MD
    2 days ago
  • 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

    Emmes

    Rockville, MD
    6 days ago
  • 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... 
    Regulatory
    Remote job

    Syneos Health/ inVentiv Health Commercial LLC

    Washington DC
    5 days ago
  • $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... 
    Regulatory
    Remote work
    3 days per week

    Piper Companies

    Bethesda, MD
    4 days ago
  • 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

    Emmes

    Rockville, MD
    5 days ago
  •  ...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... 
    Regulatory
    Interim role
    Local area
    Remote work

    Parexel

    Washington DC
    5 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to In-House Clinical Research Associate — TMF & Regulatory. Be the first to apply!