Viewing 1 - 10 of 21 jobs
1) Manage and co-ordinate development and trial projects 2) Review of site visit reports and correspondence with trial sites 3) Proactively identify project risks and resolves with some supervision 4) Ensure CRA resources meet site...
1) Design and develop new products and processes in accordance with market demands 2) Optimize production by analyzing processes and identify process conditions 3) Measure and evaluate progress and results for all projects as well as the...
1) Manage and coordinate department activities and systems as interface with contractors, manufacturers, packagers, laboratories in the management of current product portfolio and development of new products projects effecting regulatory...
Partial Job Description 1) Write statistical methods and results sections of reports 2) Review draft reports for consistency and completeness 3) Communicate effectively with senior statisticians and clinicians within the team 4) Perform...
1) The Associate Director, Drug Safety and Pharmacovigilance position plays a key role in setting executing departmental strategy, as well as managing the day-to-day functioning of the department. 2) Oversees all departmental activities...
1) Pursue new prospects (cold calling, attending professional meetings, seminars, conferences and meeting with potential clients) 2) Present product development and analytical services to clients 3) Create collateral marketing materials 4)...
1) Update clinical trial management systems 2) Manage distributing, tracking, filing, processing and archiving of clinical trial materials in accordance with SOPs, including such things as adverse events, patient data, laboratory reports,...
Serve as Senior Engineer for major medical device development projects. Ensure that engineering design activities are coordinated per the development procedure. Work closely with electrical and software engineers, designing with...
1) Ensure every detail of the trial instructions is followed without fluctuation or error as any variance may render the study invalid 2) Prepare daily or weekly reports on the details of the trial's progression and details that are...
1) Conduct site visits (initiation, monitoring, termination) 2) Adhere to FDA, ICH-GCP regulations and local regulations 3) Ensure completion and collection of SAEs 4) Instruct the site staff in their roles and responsibilities in...