A pharmaceutical project manager has to oversee clinical trials and coordinate the development of clinical products.He has to develop the budget required for performing clinical trials.He has to plan the time schedule and quality guidelines for the clinical trails.He also has to ensure that these guidelines are being met by the departments concerned.He has to involve himself in selecting the medical research organizations that would be conducting clinical trials.He has to coordinate with members of the different departments who are involved in the clinical trial and make sure that the time schedules are being met.He also has to compile the data of the trial.He has to make sure that the clinical trial meets the company’s goals and objectives

Documentation SpecialistResponsibilities:Responsibility for the timely, accurate, and efficient management of documents including access and revision control.Manage “Live” Documentation updates from the Operations floorTurnaround and issue documentation as per Operations ScheduleManage and implement on the floor documentation control systemDrive the Documentation Life Cycle System to ensure documents are approved in as per Scheduling requirements.Work with various Subject Matter Experts to ensure technical documentation updates are approved.Creation and revision of Standard Operating Procedures (SOPs) Work Instructions (WI’s) as requiredWork closely with QA, Supply chain and Operations core functionsEnsure compliance with all regulatory GMP, Safety and Environmental requirements.

Documentation SpecialistResponsibilities:Responsibility for the timely, accurate, and efficient management of documents including access and revision control.Manage “Live” Documentation updates from the Operations floorTurnaround and issue documentation as per Operations ScheduleManage and implement on the floor documentation control systemDrive the Documentation Life Cycle System to ensure documents are approved in as per Scheduling requirements.Work with various Subject Matter Experts to ensure technical documentation updates are approved.Creation and revision of Standard Operating Procedures (SOPs) Work Instructions (WI’s) as requiredWork closely with QA, Supply chain and Operations core functionsEnsure compliance with all regulatory GMP, Safety and Environmental requirements.