Natco Pharma Limited – Hiring for Clinical Trials / Pharmacovigilance Departments

 

Natco Pharma Limited is a vertically integrated and R&D focused pharmaceutical company engaged in developing, manufacturing and marketing of finished dosage formulations (FDF”) and active pharmaceutical ingredients (“APIs”). Natco Pharma Limited was incorporated in the year 1981 and today has eight manufacturing facilities spread across India consisting of over 4500 employees. Our focus is primarily on niche therapeutic areas and complex products. We market and distribute our products in over 50 countries.

!! Greetings from Natco Pharma Limited!!

We are looking for our Clinical Trials / Pharmacovigilance departments.

Job Description: Clinical Research and Drug Development

• Position Title: Clinical Research Associate
• Education: Pharm. D. or M. Pharm. (Pharmacology or Clinical Pharmacy) with good English communication skills
• Experience: 3 – 6 years’ experience preferred

Essential Functions: Coordinates with Contract Research organization and monitors investigator sites should have problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks.

• Good knowledge and experience in conducting Phase-I, II, III & IV clinical trials and Bioequivalence studies (Healthy and Patient based studies).
• Coordinate with Manufacturing facility/regulatory department with regard to investigational product labelling and other required documentation.
• Good knowledge on requirements per ICH-GCP, US FDA clinical trial regulations, New Drugs and Clinical Trial Rules 2019.
• Should have skills pertaining to the development of clinical study protocol, informed consent forms, investigators brochure and various clinical trial designs.
• Should have experience in reviewing the clinical trial reports, tables, figures etc.,
• Should be willing to travel anywhere in India.

 

Job Description (Pharmacovigilance):

• Position Title: Drug Safety Executive/Pharmacovigilance Executive
• Department: Pharmacovigilance Department
• Education: Pharm. D., with good English communication skills
• Experience: 3 to 5 years experience preferred

Key Responsibilities: 

• 1. Evaluation, processing and ensuring timely submission of adverse drug experience reports to regulatory authorities.
• 2. Provide responses to medical information inquiries.
• 3. Medical literature review
• 4. Preparation of documents related to Risk Management Programs for drugs
• 5. Preparation of Periodic Safety Update Reports
• 6. Interact with various internal departments regarding safety updates

Interested candidates can you share their profiles to jhansi@natcopharma.co.in

Note: Preferable Male Candidates