3. Intern / Trainee - Pharmaceutical Drug Safety & Pharmacovigilance


     Role and Responsibilities

  • Survey of Good Pharmacovigilance Practice Guidelines in India & Other Markets.
  • Preparing of Comparative Reports on Pharmacovigilance Practices.
  • Study the Regulatory requirements of different countries related to Pharmacovigilance and prepare comparative reports/charts/presentations. 
  • Build database based on MS Excel, to capture Regulatory requirements for Pharmacovigilance.
  • Learn PSUR, and Adverse Drug Reaction Reporting for Pharmaceuticals & Medical Devices. 
  • Prepare PV documents under guidance to senior team membersType your paragraph here.

​​​Senior Research Fellow (SRF)

  • ​Location: Bhubaneswar, India 
  • Provisions: The fellowship has tenure of 18months. And, provides Fellow's support (stipend) commensurate with National Standards (e.g. ICMR, India).
  • Qualification: Post-graduate in Bioengineering or Mechanical Engineering
  • Desirable experience: 
  1. Design and Fabrication of Microfluidic systems using polymers, glass or silicon. Techniques of chemical etching, laser cutting, photolithography and embossing/mold techniques.​
  2. Concepts of fluid mechanics, flow rates and pressure with the flow cytometry techniques.
  3. ​It is preferable that candidate has background knowledge of various Paper Based point of care Devices like Lateral Flow Devices, µPads and Enzyme-Linked-Immunoassays (paper based platforms) and the principles of general immunoassay tests.
  4. ​Demonstrated track record to lead a biomedical research program.

1. Intern / Trainee - Regulatory Affairs


     Role and Responsibilities

  • Keep updated on various regulatory development mainly with respect to South Asia, CDSCO, ASEAN countries for Pharmaceuticals, medical device & biological
  • Help in collecting, review and compilation of scientific materials for regulatory compilation & Prepare expert scientific summary for regulatory submissions. Read, review & compile ICH-CTD.
  • Learn various aspects of ICH Module 3 (Chemistry Manufacturing), Module 4 (non clinical data) and Module 5 (clinical data), with an objective to use the knowledge appropriately under guidance.
  • Work closely with business development and support business development in preparing scientific and regulatory part of communications to potential clients and established clients
  • Any other that may be based on the Company requirements, your performance, etc. Type your paragraph here.

Clinical Research Coordinator (R&D)

  • ​Location: Bhubaneswar. Duration: 6 months. 
  • Basic Stipend: Based on Qualification/Merits.
  • Initial Probation: 2 weeks to find out Candidates Suitability and Attitude     towards work.
  • Job Confirmation: Based on Internship Performance Evaluation.
  • Desirable Qualification: MSc (Chemistry, Biotechnology, Biochemistry); BPharm /MPharm; Engineering; MBA with Science Background.
  • Email: in@transintegra.in

​​Interns / Trainee

  • ​Location: Bhubaneswar, India. Job requires short travels within India. 
  • Provisions: The position is for Alzheimer's disease project, tenure of 18 months.
  • Qualification: Post Graduate in Science or Graduate in Nursing
  • Expertise & experience: 
  1. Strong written & verbal communication skills.​
  2. Ability to read & understand medical / scientific journals. 
  3. Ability to make precise & correct summary of full-text medical journals/scientific publications.
  4. Well organized with ability to track / manage stake-holders / project.
  5. Desirable that candidate has prior experience of Clinical Trials.

2. Intern / Trainee - Pharmaceutical Quality Assurance

     Role and Responsibilities

  • Survey of Good Manufacturing Guidelines in India & Other Markets. 
  • Preparing of Comparative Reports on GMP Practices. 
  • Study the Regulatory requirements of different countries, and prepare comparative reports/charts/presentations. 
  • Site Visit to Manufacturing Plants of Indian Pharmaceutical Companies. Based on successful demonstration of performance. 
  • Build database based on MS Excel, to capture Regulatory requirements for Quality Assurance / GMP, for Pharmaceutical Manufacturing Sites.