Skill required: Clinical - Medical Monitoring
Designation: Statistical Programming Scientist
Job Location: Bengaluru
Qualifications: BE/BTech/Bachelor of Pharmacy/Master of Pharmacy
Years of Experience: 5 to 8 yearsWhat would you do?
You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life- enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. You will be working as a part of the Study Startup team which is responsible for Project Initiation, Planning, Implementation, Control & Evaluation and Close-Out activities which includes initiation of trial capacity, trial setup activities, etc. You will be expected to provides medical expertise for trial oversight and safety concerns. This includes creation, review and validation of protocol requirement specifications as per the applicable SOP.What are we looking for?Adaptable and flexible Ability to perform under pressure Ability to work well in a team Written and verbal communication
Roles and ResponsibilitiesIn this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts