Biostatistician @ Biocon, Bangalore
Job Category Medical/Healthcare/Bio-Tech
Posted On 25-Nov-2011
Be responsible for all statistical tasks with a high level of independence e.g. clinical trial design/planning, sample size estimations, analysis plan, defining safety, efficacy and exploratory endpoints, reporting activities including exploratory analyses and additional analyses to support publications, plus statistical consultation during the running phase.
May be assigned to lead a small project or parts, initially under the guidance of a more experienced statistician, but with increasing autonomy and accountability.
Ensure timeliness and adequate quality of all deliverables for the assigned trials and project tasks.
Able to manage CRO deliverables.
Follow processes and adhere to Health Authority requirements (SOP's, NIP's, Master Analysis Plan, GCP and regulatory guidelines) and write SOPs.
Establish and maintain sound working relationships and effective communication within the Clinical Trial Team/International Clinical Trial Team and the Statistics team.
Closing date: Contact employer