Natco Pharma Walk In Interview 2023.Natco Pharma Notification full details below..Interested and eligible candidates can attend interview on scheduled time and venue.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”). Our focus is primarily on niche therapeutic areas and complex products.
Vacancy details:
- Department: Pharmacovigilance/Clinical Research and Drug Development
- Position Title: Drug Safety Executive/Pharmacovigilance Executive/Clinical Research Associate
- Qualification :Pharm. D. or M. Pharm. (Pharmacology or Clinical Pharmacy) with good English communication skills
- Experienced:3 to 6 years experience preferred
Job Description: !! Greetings from NATCO PHARMA LIMITED !!
Important Details :
- Location: Hyderabad/Secunderabad
- Post of date:24/06/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
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
