Clinical Affairs

Year    TN, IN, India

Job Description

Age limit:20 to 30.

Clinical Study Design & Execution:

Leading the design and implementation of clinical study protocols and monitoring their progress.

Regulatory Compliance:

Ensuring all activities, from clinical trials to post-market evaluations, adhere to regulatory requirements and guidelines (e.g., FDA regulations, GCP).

Data Management & Analysis:

Overseeing the collection, interpretation, and reporting of clinical data to ensure its accuracy and integrity.

Cross-Functional Collaboration:

Working with various departments, including R&D, regulatory affairs, quality, risk management, and marketing, to integrate clinical strategy with product development.

Investigator & Site Management:

Recruiting and managing relationships with clinical trial investigators and research sites.

Regulatory Submissions:

Preparing the clinical sections of documents for regulatory submissions and providing clinical information for other reports.

Product Lifecycle Support:

Providing scientific evidence and insights throughout the product's lifecycle, including during post-market surveillance.
Job Types: Full-time, Permanent, Fresher

Pay: ₹38,160.05 - ₹52,536.72 per month

Benefits:

Food provided
Work Location: In person

Beware of fraud agents! do not pay money to get a job

MNCJobsIndia.com will not be responsible for any payment made to a third-party. All Terms of Use are applicable.


Job Detail

  • Job Id
    JD4318122
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    TN, IN, India
  • Education
    Not mentioned
  • Experience
    Year