Clinical Data Associate (Ascentrik)

5/28/20261 min read

Roles and Responsibilities

Key Accountabilities / Responsibilities:

  • Strong knowledge of various phases and types of clinical trials.

  • Good understanding of efficacy, safety, biomarker expressions, bioavailability, CMC, Mechanism of Action and Interventions.

  • Understanding of pathophysiology, treatment/therapies of cancer, various genetic, autoimmune and neurological disorders.

  • Organizing and monitoring the different phases of clinical trials of different drugs and track & coordinate changes.

  • Understanding of clinical trial sources and different trial registries.

  • Collecting and authenticating data from conferences and publications.

  • Keep a regular track on the updates in trials/reports using multiple sources.

  • Excellent knowledge about websites like Pub Med, Clinicaltrials.gov, Abstracts, Annual reports etc.

  • Quick learner and ability to grasp new technologies.

  • Should be able to conduct 100% quality check of all the documents, rectifying the errors before submitting the work for execution.

  • Must be able to work in a deadline driven environment & be able to handle various assignments.

Qualifications / Requirements:

  • Master of Pharmacy (Pharmaceutics, Pharmacology etc.) or Master of Science (Biotechnology, Biochemistry, Molecular Biology, Microbiology, Clinical Research, Drug Development, Genetics, Immunology etc.).

  • Not Eligible / Exclusions: M. Pharm Candidates with a major in Pharmacognosy or M.Sc. Candidates with a major in Botany, Zoology, Environmental Science or Ecology.

  • Preference is for Candidates with a Master’s degree however Candidates with a Bachelor of Pharmacy Degree and minimum 1 year of relevant experience in fields such as Clinical Research, Pre-Clinical Research, Drug Development, Clinical Trial Management, Clinical Data Management or Medical Writing can be considered.

  • Post Graduate Diploma in Clinical Research or Clinical Data Management would be an asset.

  • Ideal candidate would have strong scientific understanding and familiarity with drug development processes in the field of cancer and other immunological disorders.

  • Familiarity with pre-clinical and clinical studies.

  • At least one research paper published in a peer-reviewed journal.

  • Good proficiency in handling Excel and other analytical tools.

  • Secondary research experience.

  • Excellent written and verbal communication skills.

  • Inquisitive mindset and a dedication to continuous learning & improvement.

Location:

Pune (Wakad), Maharashtra.

To apply please email your Resume to dixit.chaitali@ascentrik.com
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