Clinical Research Associate / Clinical Research Specialist / Clinical Trial Coordinator

Company: Microsoft Learn Student Ambassador - Women Tech Hub

  • Location: Frankfurt, Germany
  • Seniority: Entry level
  • Employment type: Part-time
  • Posted: 14 days ago
  • Offer language: English

Job description

Role Description

We are seeking a Clinical Research Associate / Clinical Research Specialist / Clinical Trial Coordinator to support clinical study delivery, site coordination, and research quality. You will work with investigators, sponsors, and study teams to help conduct trials according to approved protocols and applicable requirements.

Key responsibilities include:

  • Support study feasibility, site initiation, ongoing conduct, and close-out activities.
  • Coordinate study visits, schedules, documentation, and communications.
  • Support participant recruitment and informed consent processes within assigned responsibilities.
  • Review study data and documentation for accuracy, completeness, and protocol adherence.
  • Conduct or support site monitoring activities, as appropriate to the role.
  • Maintain essential study documents and support ethics submissions.
  • Track protocol deviations, safety reporting workflows, and corrective actions.
  • Coordinate with investigators, sponsors, laboratories, and other study partners.
  • Support audit readiness and timely resolution of study queries.

Qualifications

  • Bachelor’s degree in Life Sciences, Nursing, Pharmacy, Medicine, or a related field, or equivalent relevant experience.
  • Experience in clinical research, trial coordination, or clinical site monitoring.
  • Working knowledge of Good Clinical Practice, research ethics, and clinical trial processes.
  • Familiarity with electronic data capture systems and clinical trial management tools.
  • Strong organizational skills, attention to detail, and documentation practices.
  • Clear communication skills and the ability to collaborate with clinical and research teams.
  • Commitment to participant confidentiality, safety, and ethical research.
  • Relevant clinical research certification is an advantage.

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