Sr. Clinical Data Associate

Position Summary

• We are looking for a Senior Clinical Data Associate who will be working on building and maintaining a drugs, clinical trials, deals & companies’ intelligence database based on modular solutions focusing on various therapeutic areas.

• The content is manually curated by researchers providing in-depth data to help identify the most relevant trends in the landscape. You will be part of a global network of life science researchers working on dynamic, fast growing products in exciting, cutting-edge life science areas.

Key Accountabilities / Responsibilities

• Lead and manage researchers in order to curate accurate, timely, insightful and comprehensive data and intelligence

• Identify and analyze the most relevant information for the database and its users

• Daily target planning based on influx of data volume

• Regular quality checks as per SOPs on data extracted by researchers to achieve quality benchmark

• Manage the daily activities aligned for team’s productivity and quality

• Generate queries to clarify and improve the quality of the data

• Analyze and present the quality data for team and create improvement plan as required

• Independent work on specified projects as per SOP

• Review and implementation of SOPs along with continuous process improvement

• Cross-team collaboration

• Coordinate with UK based Clients on a regular basis to understand and meet the project deliverables

• Manage the activities required towards the launch of the database modules and further support the needs towards maintenance post launch.

• Tracker maintenance and update

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

• 2 to 4 years of relevant life sciences experience in fields such as Clinical Research, Pre-Clinical Research, Drug Discovery & Development, Clinical Trial Management, Clinical Data Management or Medical Writing

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

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

• Familiarity with pre-clinical and clinical studies

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

• QC skills

• Good proficiency in handling Excel and other analytical tools

• Secondary research experience

• Good project management and people management skills are highly desirable

• Excellent written and verbal communication skills

• Good reporting skills

• Inquisitive mindset and a dedication to continuous learning & improvement

• Preference is for experienced Candidates with a Master’s degree however Candidates with a Bachelor of Pharmacy Degree and minimum 2 years of relevant experience along with a Post Graduate Certificate/Diploma in Clinical Research can be considered