A Clinical Study Manager job position has opened up at an international contract research organisation providing drug discovery, lifecycle management and laboratory services. With offices in over 45 countries and approximately 13,000 professionals, this company provide innovative ideas behind multiple sectors. This particular position will be based in West London, UK on a contract basis. This role will include negotiable rates and flexible working.
- This study manager position is accountable for achieving the final clinical deliverable within the time period specified in the contract with the Customer.
- The CTM will be able to interpret data on project issues and make good business decisions with support from experienced team members or line management.
- Maintains profitability by ensuring clinical activity is conducted within contract scope, through efficient management of the clinical team
Responsibilities may include:
- Manages all clinical operational and quality aspects of allocated studies in compliance with ICH GCP.
- Develops Clinical tools e.g. Monitoring Plan, Monitoring Guidelines in conjunction with Data Quality Plan.
- Responsible for timely set up, organization, content and quality of the relevant sections of the Trial Master File
- May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates, etc.
- In conjunction with the project manager prepares, organizes and presents at Investigator Meetings.
- Responsible for the implementation and training of standardized clinical monitoring processes according to corporate standard policies.
- Responsible for the timely archiving of documents and study materials for the clinical department.
- Monitors clinical activity timelines and metrics.
- Provides regular status updates to PM for client reports.
- Ensures regular project review, using company tracking & management tools, implementing appropriate recovery actions to ensure project timelines are met.
- Reviews monitoring visit reports and ensures finalization is within contractual timeline.
- Manages CRF collection and query resolution process
- Monitors /co-monitors clinical trials as needed to assess performance and/or ensure contractual obligations are met.
- Leads regular conference call meetings with monitors and other clinical team members.
- May participate in bid defense meetings.
Education and Experience:
- Bachelor's degree or licensed certified health care training
- Significant clinical research experience (comparable to 3 years) in all phases of study life cycle, including start up, interim and close out
- Previous experience as a field CRA (preferred)
- CRO/Pharma experience (preferred)
- Valid Driver's License and Passport
- Or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Matthew Pike on +44 207 4400 639 or upload your CV on our website www.proclinical.com.
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.