Colmar / Alsace (France)
PPRS is an independent and fast-growing company, specialized in the development of innovative projects with diagnostic or therapeutic purposes in neurosciences.
Under the responsibility of the Director of Clinical Operations , you will be responsible to provide the operational expertise to ensure the effective and efficient delivery of all operational aspects of one or more studies through all phases of clinical Study Management (Plan, Initiate, Conduct, Close), in accordance with the appropriate quality standards including ICH/GCP and applicable regulations . The suitable candidate achieves this by delivering high quality study management support and other high value services to enable team and project success.
-Participates in the planning, development and execution of clinical trials:
-Assist in Management of clinical studies including investigators selection, analysis of potential patient recruitment, organizing and leading investigator meetings as well as developing key study documents (protocols, relevant source documents, informed consents, clinical trial agreements, Monitoring Plan).
-Ensures that studies are conducted with full adherence to the study protocol, SOPs, applicable regulations, and principles of Good Clinical Practice (GCP).
-Contribute to develop the clinical study budget
-Ensure clinical studies are conducted in a timely manner and within predefined budgets
-Communicates with external vendors. Ensure timely delivery and reviews of documents generated by external parties.
-Contribute to the Quality Control of all deliverables received from external parties.
-Coordinates the scheduling of all trial-related conference calls
-Responsible for assisting in the development, implementation, maintenance and archiving of Clinical Trial Master File
-Perform Site-study initiation, interim monitoring and close out visits as required
-Ensure and assure quality of the data collected on site according to ICH-GCP, SOP and study protocol
-Assist our Project Manager on assigned projects and will take a lead role where required
-Coordinate responses to study questions or issues from Health Authorities or IRBs/IECs
-Responsible for the preparation of reports, documents, statistical surveys and other such data as required.
-Assumes additional responsibilities as needed, with little or no supervision.
-Provides support to other positions as needed.
-Assists Directors in the creation and maintenance of internal policies and SOPs.
Colmar / Alsace (France)
Negotiable, depending on experience