Senior Clinical Research Associate
1 week ago
Job Summary
We are seeking a highly skilled and experienced Senior Clinical Research Associate to join our team at PRA Health Sciences. As a Senior Clinical Research Associate, you will be responsible for monitoring and managing clinical trials in the pharmaceutical industry, with a focus on oncology trials.
Key Responsibilities
- Monitor and manage multiple clinical trials, ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements.
- Develop and maintain strong relationships with investigators, site staff, and other stakeholders to ensure successful trial execution.
- Conduct site initiation visits, monitoring visits, and close-out visits to ensure trial integrity and data quality.
- Identify and report any deviations or issues related to trial conduct or data quality.
- Collaborate with cross-functional teams, including clinical operations, data management, and biostatistics, to ensure trial success.
- Develop and maintain knowledge of clinical trial regulations, guidelines, and industry standards.
- Stay up-to-date with industry trends and developments, and apply this knowledge to improve trial design and execution.
Requirements
- Minimum of 3 years of experience in clinical research, preferably in the pharmaceutical industry.
- Minimum of 1-3 years of experience in monitoring oncology trials.
- Strong knowledge of GCP, ICH guidelines, and local regulatory requirements.
- Excellent communication and interpersonal skills, with the ability to work effectively with investigators, site staff, and other stakeholders.
- Ability to travel up to 50% of the time, with occasional overnight stays.
- Strong analytical and problem-solving skills, with the ability to identify and resolve issues related to trial conduct or data quality.
What We Offer
- Competitive salary and benefits package.
- Opportunities for professional growth and development.
- Collaborative and dynamic work environment.
- Recognition and rewards for outstanding performance.
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