Clinical Research Associate
Vor 3 Tagen
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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