
Senior Clinical Data Associate
3 days ago
Position Summary:
• We are looking out for a Senior Clinical Data Associate who will be working on Beacon Targeted Therapies (https://beacon-); a database from our UK based Client, Hanson Wade.
• Beacon is 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 Beacon 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 teams 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 Beacon modules and further support the needs towards maintenance post launch.
• Tracker maintenance and update
Qualifications / Requirements:
• Master of Pharmacy (Pharmaceutics, Pharmacology etc. except Pharmacognosy) or Master of Science (Biotechnology, Biochemistry, Molecular Biology, Microbiology, Clinical Research, Drug Development, Genetics, Immunology etc.)
• 2 to 4 years of relevant life sciences experience in fields such as Clinical Research, Pre-Clinical Research, Drug 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 Masters 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
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