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Clinical Research Associate Ii

CRA II: Minimum 2+ years of CRA experience in the CRO or pharmaceutical industry Senior CRA: 3+ yea years
not specified
10 Sept. 5, 2025
Job Description
Job Type: Full Time Education: 4-year college degree or equivalent experience (scientific or healthcare discipline preferred) Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title:

Clinical Research Associate II (CRA II)

Location:

Remote – Netherlands

Job Type:

Regular Full-time

Division:

Precision for Medicine

Business Unit:

Clinical Solutions

Requisition Number:

4666


About Precision for Medicine

Precision for Medicine is not your typical CRO. We combine deep scientific knowledge, operational scale, and cutting-edge technologies to accelerate the development of life-changing therapies. What truly sets us apart is the integration of clinical trial execution with laboratory expertise and advanced data sciences.

We are proud of our high CRA retention rates, supportive culture, and meaningful work-life balance.


Position Summary

As a Clinical Research Associate II, you will take ownership of monitoring and managing the progress of clinical studies at investigative sites. You will ensure all aspects of the study are conducted, documented, and reported in accordance with protocol, SOPs, ICH-GCP, and applicable regulations.

CRAs at Precision enjoy:

  • Lower protocol volume – allowing you to become a protocol expert.

  • Reasonable travel – typically 50–60%, with improved work-life balance.

  • A voice that matters – at a smaller CRO, your impact is direct and your ideas are heard.

  • Supportive leadership and career growth opportunities.


Key Responsibilities

  • Monitor clinical studies at investigative sites.

  • Ensure compliance with ICH-GCP, protocol, and regulatory guidelines.

  • Conduct pre-study, initiation, routine, and close-out monitoring visits.

  • Coordinate study start-up activities, including regulatory submissions and investigator selection.

  • Identify potential study risks and proactively propose mitigation strategies.

  • Maintain high quality documentation and site communication.

  • Participate in project team updates and site management planning.

  • For senior CRAs:

    • Train and mentor junior CRAs.

    • Support Project Managers with large-scale trials.

    • Initiate site payments and assist in proposal development and client presentations.


About You

You:

  • Stay calm, thoughtful, and responsive under pressure.

  • Are prepared and proactive—always two steps ahead.

  • Are creative in overcoming site and protocol challenges.

  • Have an exceptional eye for detail and a strong sense of ownership.

  • Communicate clearly and resolve conflicts with professionalism.

  • Are passionate about advancing oncology research.


Minimum Qualifications

  • Education:

    • 4-year college degree or equivalent experience (scientific or healthcare discipline preferred)

  • Experience:

    • CRA II: Minimum 2+ years of CRA experience in the CRO or pharmaceutical industry

    • Senior CRA: 3+ years CRA experience with larger study responsibilities

  • Clinical Experience:

    • Oncology experience is required

    • Experience with study start-up activities preferred

  • Travel:

    • Willingness to travel domestically up to 50–60% (international travel may be required for some roles)


Preferred Qualifications

  • Graduate or postgraduate degree in scientific/healthcare field

  • 2+ years of oncology-specific monitoring experience

  • Financial management experience (for Senior CRA roles)


Why Join Us

At Precision for Medicine:

  • You'll work on groundbreaking cancer therapies.

  • You’ll be part of a team where your ideas matter.

  • You'll have the opportunity to grow while being supported and appreciated every day.


Important Notice – Recruitment Fraud

We are aware of fraudulent job offers made by individuals posing as Precision for Medicine representatives. Please note:

  • We do not extend offers without communication from our official recruiting team.

  • All legitimate job postings are available on our website.

  • Report suspected fraud to the FTC: https://www.ftc.gov


Equal Opportunity Employer

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.


Accessibility

If you require a reasonable accommodation to apply, or are unable to use our online system, please contact:
📧 QuestionForHR@precisionmedicinegrp.com