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Clinical Research Coordinator- Clinical Research Associate Home-Based

0-2 years
Not Disclosed
10 Sept. 16, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Clinical Research Coordinator – Clinical Research Associate (Home-Based)

Location: Germany
Functional Area: Clinical Research Associate
Job ID: 11245
Employment Type: Full-time
Work Arrangement: Home-based


Job Summary:

Medpace is seeking Clinical Research Coordinators to join our growing team as Clinical Research Associates (CRA). This role is ideal for professionals with at least 1 year of Clinical Research Coordinator experience. Through our PACE® Training Program, you will receive comprehensive CRA training and have the opportunity to work home-based. Generous travel bonuses and competitive salary are included.

Unexpected Rewards:

  • Make a difference on a large scale through pharmaceuticals and medical devices.

  • Dynamic, varied daily responsibilities.

  • Exposure to multiple therapeutic areas.

  • Work within a team of therapeutic and regulatory experts.

  • Defined CRA promotion and growth ladder with mentoring/management opportunities.

  • Competitive pay and travel bonuses.

CRA Perks:

  • Competitive travel bonus

  • Flexible work hours

  • In-house travel agents

  • Ongoing therapeutic training by in-house medical and regulatory experts

  • International CRA team collaboration


Key Responsibilities:

  • Conduct qualification, initiation, monitoring, and closeout visits at research sites per approved protocol.

  • Communicate with medical site staff, including coordinators and clinical research physicians.

  • Verify investigator qualifications, training, resources, and site facilities.

  • Conduct source document verification against case report form (CRF) data; ensure Good Documentation Practices (GDP).

  • Conduct on-site and virtual/remote monitoring using a risk-based approach via Clinical Trial Management System (CTMS).

  • Ensure eligibility of enrolled subjects.

  • Review regulatory documents.

  • Manage investigational product/drug and medical device accountability.

  • Review and verify adverse events (AEs), serious adverse events (SAEs), concomitant medications, and illnesses for accurate reporting.

  • Assess patient recruitment and retention and provide suggestions for improvement.

  • Complete monitoring reports and follow-up letters, summarizing findings, deviations, deficiencies, and corrective actions.


Qualifications:

  • Education: Bachelor’s degree in health or science-related field.

  • Experience: Minimum 1 year as a Clinical Research Coordinator.

  • Skills:

    • Ability to travel 60–70% within the DACH region (some visits may be remote).

    • Proficient in Microsoft Office.

    • Strong verbal and written communication and presentation skills.

    • Detail-oriented and excellent time-management.

    • Fluency in German and English.


Medpace Overview:

Medpace is a full-service Clinical Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 people across 40+ countries. The company leverages local regulatory and therapeutic expertise across oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective areas.


Why Medpace:

  • Flexible work environment

  • Competitive compensation and benefits package

  • Paid time off (PTO) and structured career growth opportunities

  • Company-sponsored employee appreciation events

  • Employee health and wellness initiatives

  • Multiple CRO Leadership Awards from Life Science Leader magazine