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Navitas Life Sciences

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3.5

based on 154 Reviews

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3 Navitas Life Sciences Jobs

Principal Investigator

1-4 years

Manipal

1 vacancy

Principal Investigator

Navitas Life Sciences

posted 4d ago

Job Role Insights

Flexible timing

Job Description

Role & responsibilities

  • Ensure that all human-subjects research is conducted in an ethical manner and in accordance with all federal, state, and local laws and regulations and institutional policies.
  • Ensuring that a clinical study is personally conducted and supervised in compliance with GCP, with the applicable regulatory requirement(s), with the protocol agreed to by the sponsor and given approval/favorable opinion by the EC and as per in house SOP.
  • Supervision and overall responsibility of all studies from end to end.
  • Significant contribution in design and development of SOPs for clinical research BA/BE studies.
  • Delegation of study specific activities to study personnel.
  • Imparting training to study personnel for study specific protocols.
  • Interaction with Ethics committee regarding protocol submission, presentation of protocol to the ethics committee and obtaining approval for the protocols.
  • Screening, Physical examination and selection of the healthy volunteers.
  • Screening and selection of the healthy volunteers.
  • Presentation and obtaining screening/study specific ICF and clarify the questions.
  • Vital signs examination during study and check-in process.
  • Management of AE and SAE.
  • Apply Inclusion/Exclusion criteria for selection of healthy subjects for the study.
  • Monitoring the entire study process.
  • Post study report analysis, documentation, follow up.
  • IP receipt, Accountability, dispensing, archival and retrieval.
  • Various Regulatory Compliance.
  • In charge of all clinical logbooks.
  • CAPA Response to QA/Sponsors observation / queries.
  • Personally, conducting or supervising the conduct of human-subjects research and for protecting the rights, safety, and welfare of the subjects enrolled in the research in compliance to GCP.
  • Facing various regulatory/Sponsor audit
  • Ensure clinical studies are conducted as per agreed timeline and meet customer satisfaction

Preferred candidate profile

MBBS or MD Pharmacology qualification with relevant experience in conducting BA/BE studies.


Employment Type: Full Time, Permanent

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What people at Navitas Life Sciences are saying

What Navitas Life Sciences employees are saying about work life

based on 154 employees
74%
77%
64%
100%
Flexible timing
Monday to Friday
No travel
Day Shift
View more insights

Navitas Life Sciences Benefits

Health Insurance
Cafeteria
Work From Home
Soft Skill Training
Team Outings
Job Training +6 more
View more benefits

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