Abbott is about the power of health. For more than 125 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 150 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health.
Post: Clinical Project Lead
Job Description:
• Develop study management plans, together with team assignments and accountability and oversight of database and study maintenance.
• To provide appropriate information for local and central tracking systems within required timelines
• Serve as primary project contact with vendors to ensure communication is maintained and reporting and tracking schedules are adhered to through study execution phase.
• Manage and co-ordinate with cross-functional project teams to support milestone achievement and to manage study issues and obstacles and ensure compliance with standard processes, policies and procedures.
• Maintain appropriate communication with relevant functional areas
• To anticipate and proactively solves study-related clinical site issues as they occur and initiates, recommends and communicates corrective action as indicated. Use functional expertise and exercise good judgement in seeking appropriate guidance and ensure that follow-up to any and all corrective action is taken at the clinical site and is properly documented
• Undergo and maintain training as required by the functional role and other relevant company procedures, to ensure adherence to ICH-GCP, Abbott SOPs, processes and procedures, local Work Instructions (if any), applicable regulatory requirements and study specific needs
• Provide input for the development of proposals and study documents for clinical studies and manage project budgets.
• Contribute to achieving satisfactory study audits internal and external
• Forecasting budget for assigned studies and keeping a track on planned actual expenditure for assigned studies to ensure the study budgets are on track. • Vendor management
• Maintain at most quality for study related documents and all the clinical trial activities performed
• Forecasting study milestones of assigned clinical trials and accomplishing deliverable as per the planned milestones
• Mentoring juniors and interns (if any) at Abbott India Limited for activities related to clinical research
• Ensure together with line manager appropriate delegation of study related responsibilities during absence
Candidate Profile
• M. Pharm/ B. Pharm/MSc/BSc with PGDCR/ Medical, pharmacy or life-sciences degree (or equivalent)
• Minimum 4-5 years of work exp. in various capacities for clinical research in MNC CRO or MNC Pharmaceutical Company.
• Previous experience of working within the pharmaceutical industry and, in particular, Pharmacovigilance is preferred, but not mandatory.
Additional Information:
Qualification : M. Pharm/ B. Pharm/MSc/BSc
Exp : 4-5 years
Location: Mumbai
Industry Type: Pharma/ Biotech/Clinical Research
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