Teva Freshers R&D Intern Vacancy - B Pharma/M Pharma Candidates Apply

Teva Freshers R&D Intern Vacancy – B Pharma/M Pharma Apply

Teva announces job opening for pharma freshers candidates. Candidates with bachelor’s and master’s degree on pharma may apply for the job opening at Teva. Teva hiring, B Pharma job opening 2023, M Pharma job opening 2023. B Pharma job. Teva pharma job opening 2023. Intrested and eligible candidates may check out all the details on the same below:

Job Title: R&D Intern

Job Id: 46858

Location: Navi Mumbai, India, 400706

Eligbility Criteria: 

Education: B. Pharm, M. Pharm or M.Sc. (Clinical Research).

Experience: 0-2 years of experience as a Clinical Research Coordinator in reputed BA/BE center.

Total years of experience required for the role: 0-2 years

Function Research & Development

Sub-Function Drug Development and Preclinical Studies

Job Description

  • Overseeing the smooth running of BA/BE studies.
  • Collecting, compiling, completing and reviewing data obtained from research.
  • Informing participants about study during ICF process.
  • Get involved in the Investigational product administration process.
  • To act as a custodian and monitoring of research participants to ensure adherence to study rules.
  • Adhering to research regulatory standards and in-house SOPs.
  • Adhering to ethical standards like ICH-GCP and GLP.
  • Maintaining detailed records of studies as per FDA and other required guidelines, including things such as drug administration and subject specific case report forms.
  • Co-ordination with pathology laboratory regarding screening, post study and follow up sample analysis.
  • Ensuring that the necessary supplies and equipment for a study are available before initiation of study.
  • Engaging with study staff for timely completion of study documentation to meet stringent timelines of project submission.
  • Collects data as required by the protocol. Assures timely completion of Case Report Forms.
  • Maintains study timelines.
  • Completes study documentation and maintains study files in accordance with requirements as per in house SOPs and procedures including, but not limited to, consent forms, source documentation, case report forms and investigational material accountability forms (if required).
  • Engaging with subjects and understanding their concerns.

Apply Online

Important Interview Questions and Answers for the above job role:

  1. What inspired you to apply for this R&D Intern position, and what relevant skills and experiences do you have?

Answer: As a recent B.Pharm/M.Pharm/M.Sc. graduate with an interest in clinical research, I am excited about this opportunity to contribute to drug development and preclinical studies. During my studies, I gained hands-on experience in clinical trial management, data collection, and analysis. In addition, I have excellent communication and organizational skills, as well as proficiency in data management software.

2. Could you describe your understanding of BA/BE studies, and how would you ensure their smooth running?

Answer: BA/BE (bioavailability/bioequivalence) studies are conducted to determine the efficacy and safety of a new drug by comparing its performance with an existing drug. To ensure the smooth running of such studies, I would first review the protocol and familiarize myself with the study objectives, inclusion/exclusion criteria, and timelines. I would also ensure that all necessary supplies and equipment are available before initiating the study, and work closely with the pathology laboratory to coordinate screening, post-study, and follow-up sample analysis. During the study, I would monitor research participants to ensure adherence to study rules, collect and compile data as required by the protocol, and maintain detailed records of the study as per FDA and other required guidelines.

3. How familiar are you with ICH-GCP and GLP guidelines, and how would you ensure adherence to ethical standards during the study?

Answer: ICH-GCP (International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use – Good Clinical Practice) and GLP (Good Laboratory Practice) are essential ethical and quality standards for conducting clinical research. I am familiar with these guidelines and have followed them during my previous clinical research experience. To ensure adherence to ethical standards during the study, I would inform participants about the study during the ICF (Informed Consent Form) process, act as a custodian and monitor of research participants, and adhere to research regulatory standards and in-house SOPs. I would also engage with study staff and subjects to address their concerns and ensure timely completion of study documentation.

4. What challenges have you faced during your previous clinical research experience, and how did you overcome them?

Answer: During my previous clinical research experience, I faced challenges such as managing study timelines, coordinating with study staff, and ensuring data accuracy and completeness. To overcome these challenges, I developed excellent time management and communication skills, collaborated closely with study staff, and implemented quality control measures to ensure data accuracy and completeness. I also maintained detailed records of the study as per FDA and other required guidelines.

5. What are your career goals, and how do you see this R&D Intern position helping you achieve them?

Answer: My career goal is to become a successful clinical research professional and contribute to the development of new and innovative drugs. This R&D Intern position would provide me with an excellent opportunity to gain hands-on experience in drug development and preclinical studies, learn from experienced professionals in the field, and develop essential skills such as data management, study coordination, and adherence to ethical and regulatory standards. I believe that this internship would help me achieve my career goals and prepare me for a successful career in clinical research.

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