We are looking for motivated Clinical Operations Associates to support the planning, coordination and execution of clinical research activities while ensuring compliance with clinical trial protocols and regulatory guidelines.
Key Responsibilities:
Assist in coordinating clinical trial activities and site operations.
Maintain clinical trial documentation and records.
Support informed consent and regulatory documentation processes.
Ensure compliance with ICH-GCP guidelines and study protocols.
Coordinate with investigators, research teams and other stakeholders.
Track study progress and assist with clinical trial reporting.
Required Skills:
Basic knowledge of Clinical Research and Clinical Trial Operations.
Understanding of ICH-GCP guidelines and clinical trial protocols.
Knowledge of TMF/ISF documentation.
Positive communication, coordination and organisational skills.
Proficiency in MS Office, especially Excel and Word.
Robust attention to detail and problem-solving abilities.
Eligibility: B.Pharm, Pharm.D, M.Pharm, B.Sc. Life Sciences, Biotechnology, Microbiology, Nursing or other relevant healthcare graduates.