, preferably within clinical research, some of which must be as a Project Manager (PM) within clinical research... Management of larger studies may occur with appropriate support. May act as overall manager... occurred. • Performs detailed project planning and forecasting to ensure all relevant steps required... of Serious Adverse Event. • Monitors workload of assigned staff and alerts the head of department
Requirements: This steadily expanding CRO is recruiting a Senior Project Manager who will have full project management responsibility for clinical studies according to Company (and/or Sponsor) SOPs, ICH-GCP and local regulations. Studies managed will usually be either
Ref 114/1910Operations Manager - Events Perm Ashby de la Zouch, Leics £39-42K + bensOperations... Manager - EventsAshby de la Zouch£39-42,000 _ BensWe are currently looking for suitable candidates to fill... profitable execution of pharmaceutical meetings, in addition provide support to the Events Team Leader... to effectively and efficiently manage and support and develop all event operations to the highest possible...Event Management
Associate to join their team on a 12 months contract. Responsible for the receipt and data entry of adverse... event reports following Company Standard Operating Procedures, internal business practices... and make suggestions for system and procedure enhancements. Project Work Audits, Inspections and other Ad... in local or global project teams Soft skill development activities *Registered Nurse and/or Health...Logistics Analyst
Experience: Experienced (Non-Manager)
Contract: Temporary / Contract
the pharmaceutical industry or clinical research organisation. • Knowledge of the clinical development process... studies within agreed project • timelines. • Communicates programming related study issues to the Study... Data Manager. • Participates in business development and client liaison as required. • Provides... as line manager for assigned Biometrics staff. • Checks departmental CVs and job descriptions are complete...Pharmaceutical
Contract: Contract
. Pharmacovigilance Medical Review Responsible for day to day medical review of all Serious Adverse Event (SAE... ) reports on the companies sponsored trials Work closely with the Pharmacovigilance Manager regarding review... into clinical trial Annual safety reports (ASRs) 2. Clinical Study Operations / Project Management To provide... medical advice to the clinical study and project teams To provide medical input into clinical trial
Contract: Contract
Ashford Canterbury Sittingbourne Folkestone Southern
Company: Jenrick-CPISalary: 30 - 55 Per Hour
pharmaceutical company in Kent to provide therapeutic area expertise and medical oversight to projects. You... will work under direct supervision of Clinical Program Lead and Project Lead Clinician. Prior experience... and following up on adverse event reports until resolution Training & education: - Must be MD, PharmD...Environmental Engineering Research Manager
Experience: Experienced (Non-Manager)
Contract: Temporary / Contract