Clinical Data Associate

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 Masters 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