In-House Clinical Research Associate I

Worldwide Clinical Trials

. Ensure quality of data submitted from study sites and assure timely submission of data .

Posted 10/5/2026full-timeRemote • Romania, Spain, PolandJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in data quality assurance, regulatory documentation, and safety event reporting within clinical research. Proficient in collaborating with diverse teams and stakeholders while maintaining a strong customer focus.

Highest-signal resume keywords

Data Quality AssuranceRegulatory DocumentationSafety Event ReportingClinical Research ExperienceProficiency in Microsoft Office

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchData SubmissionFeasibility StudiesSite IdentificationRegulatory Compliance

Soft Skills

Interpersonal CommunicationTeam CollaborationCustomer Focus

Tools & Technologies

CTMSEDC SystemsTrial Master File (TMF)

Industry Keywords

IRB ApprovalInformed ConsentLab Certification

About the role

Key responsibilities & impact

Ensure quality of data submitted from study sites and assure timely submission of data
Ensure appropriate reporting and follow-up for all safety events by site personnel
Ensure completeness and compile regulatory and ethical submission documentation, including IRB approval, informed consent, and lab certification
Provide applicable updates for site-related documentation for filing in the Trial Master File (TMF)
Perform feasibility studies and site identification activities for potential sites as requested
Collaborate remotely with clinical operations colleagues, sponsors, and site personnel

Requirements

What you’ll need

Excellent interpersonal, oral, and written communication skills
Ability to contribute to a team remotely
Strong customer focus and ability to interact professionally with a sponsor contact
Proficiency in Microsoft Office, CTMS, and EDC Systems
Four-year college curriculum with a major concentration in life science preferred but not required
Two-year college curriculum or equivalent education/training and one year experience with clinical research or other relevant experience
Proficiency in English, Romanian, and one other language: German, French, Italian, Spanish, or Polish

Benefits

Comp & perks

Equal employment opportunities regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law