Clinical Research Associate

Vor 3 Tagen


Munich, Bayern, Deutschland Allucent Vollzeit

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are seeking a highly skilled Clinical Research Associate to join our team. As a key member of our team, you will be responsible for monitoring and managing clinical trials, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.

Key Responsibilities:

  • Monitor and manage clinical trials, ensuring compliance with regulatory requirements and GCP guidelines.
  • Conduct site visits to monitor and evaluate the conduct of clinical trials.
  • Identify and report any deviations or issues related to the clinical trial.
  • Collaborate with cross-functional teams to ensure timely and successful completion of clinical trials.
  • Develop and maintain strong relationships with investigators, site staff, and other stakeholders.

Requirements:

  • At least 5 years of experience in clinical research, preferably in a monitoring or management role.
  • Relevant life science degree or healthcare background.
  • Strong knowledge of medical terminology, clinical research regulations, and GCP guidelines.
  • Excellent communication, interpersonal, and organizational skills.
  • Ability to travel up to 8 days per month, depending on project needs.

Benefits:

  • Comprehensive benefits package.
  • Competitive salary.
  • Departmental study/training budget for professional development.
  • Flexible working hours.
  • Opportunity for remote/hybrid working.
  • Leadership and mentoring opportunities.
  • Participation in our Buddy Program.
  • Internal growth opportunities and career progression.
  • Financially rewarding internal employee referral program.
  • Access to online soft-skills and technical training.


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