Clinical Research Operations Manager
2 weeks ago
We are seeking a highly skilled Clinical Research Operations Manager to join our team at Kontak Recruitment. As a key member of our clinical operations team, you will be responsible for ensuring the quality and integrity of our clinical trials.
Key Responsibilities:
- Implement and manage the quality management system (QMS) within clinical operations.
- Ensure adherence to Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and regulatory requirements.
- Oversee data quality from clinical trials, ensuring accuracy and consistency.
- Conduct quality control audits of trial sites, identifying gaps and recommending corrective actions.
Requirements:
- Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related field.
- Advanced degree (Master's or PhD) or equivalent experience in clinical research or pharmaceutical quality management.
- Minimum of 5 years of experience in clinical research, focusing on quality assurance or quality management.
- Experience as a Clinical Research Associate (CRA), ideally within a pharmaceutical company or Contract Research Organization (CRO).
- Strong familiarity with GCP, ICH guidelines, and regulatory compliance standards.
- Proven experience auditing clinical trial sites and implementing corrective actions.
- Strong communication, analytical, and problem-solving skills.
- Ability to work collaboratively in cross-functional teams.
What We Offer:
- A competitive salary and benefits package.
- The opportunity to work with a dynamic and growing company.
- A collaborative and supportive work environment.
How to Apply:
Please submit your resume and a cover letter outlining your experience and qualifications for this role. We thank all applicants for their interest; however, only those selected for an interview will be contacted.
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