We are looking for a Clinical research professional, armed with a MBBS, MD (Pharmacology/ Biochemistry/Physiology)/PhD background. Someone who has suitable years of experience in industry, preferably in Clinical Research and its management. The ideal candidate would be responsible for designing, implementing, and maintaining clinical trials along with ensuring good clinical practices being followe'd. The candidate should have experience in drafting protocols, manuscript and other scientific literature, along with demonstrated history of clinical trial management.
Job Responsibilities
Creating standards and guidelines for clinical research services and programs.
Ensuring adherence to standard operating procedures, good clinical practice and regulatory environments.
Creating a detailed research protocol that outlines the study s objectives, methodology, and ethical guidelines.
Overseeing the recruitment of study participants and ensuring that they are properly informed about the study s purpose, procedures, risks, and potential benefits.
Coordinating and managing appropriate GCP, ICH, CLIA, protocol training for team members.
Managing all regulatory documentation and correspondence required by sponsor and IRB.
Managing all planning and execution of oncology clinical trials, including decision impact and companion diagnostic trials.
Provide leadership for the clinical research teams.
Foster a positive and productive work environment.
Develop and implement the department s research strategy in alignment with organizational goals.
Stay updated on industry trends, regulations and best practices.
Ensure ethical conduct in all research activities.
Candidate should demonstrate high productivity and writing skills with a flair for writing scientific manuscripts and reports as per requirements.
Competitive salary and benefits package.
Opportunity to work in a dynamic and collaborative research environment.
Potential for professional growth and career advancement within the organization.