We are looking for a highly skilled and experienced Clinical Studies Specialist to join our team at Ruputed Pharmaceutical Company. The ideal candidate will have a strong background in clinical studies, with 2-5 years of experience.

Roles and Responsibility

- Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory requirements and company policies.

- Develop and implement study protocols, case report forms, and informed consent forms.

- Collaborate with cross-functional teams, including data management, biostatistics, and medical writing.

- Conduct site feasibility assessments and coordinate with investigators to ensure successful trial execution.

- Manage study budgets, timelines, and resources to achieve project goals.

- Ensure accurate and timely reporting of study progress and results.





Job Requirements

- Bachelor's degree in life sciences or a related field.

- Strong knowledge of Good Clinical Practice (GCP) principles and regulations.

- Experience with clinical trial management systems and electronic data capture.

- Excellent communication and interpersonal skills, with the ability to work effectively with internal stakeholders and external partners.

- Solid problem-solving and analytical skills, with attention to detail and the ability to meet deadlines.

- Ability to work independently and as part of a team, with a flexible approach to changing priorities and deadlines.

📌 Clinical Studies Specialist (Mumbai)
🏢 Naukri Healthcare Jobs
📍 Mumbai