Beschreibung
* Author of the clinical study protocol and other study essential documents.* Responsible for ordering and management of clinical trial materials, including drug supplies and CRFs.
* In collaboration with outsourcing/planning/feasibility personnel, CTT, Local CPO representatives and CRAs, identify sites and manage study set-up, including responsibility for organizing and chairing the Investigator meeting(s) (as appropriate), and/or Site Initiation meeting(s).
* Train and support the CRA(s)/CRO(s) on study protocol and related questions and serve as point of contact for managing/answering questions relating to trial procedures and subjects' eligibility.
* Ensure the set up and maintenance of the Trial Master File for assigned studies, ensuring all relevant study documents are filed and archived at the end of the study according to the appropriate guidelines.
* Chair meetings, manage team actions, and actively track study progress to ensure completion according to specified timelines, budget and quality standards. Communicate study progress to CTT, CS&I Management, CS&I TA Head and Project team representatives and others (as appropriate).
* Review and approve all study payments as per financial agreements.
* Interact with Investigator sites and CRAs/CROs/vendors to ensure smooth study set up and excellence of study conduct, reviewing site performance, protocol deviations, and maintaining awareness of issues raised.
* Assist in data review and interactions with the Data Manager, Statistician, and third parties (e.g. outsourced data management or data vendors) to ensure high quality data are transferred/available in a timely manner.
* Responsible for report writing of assigned studies either directly contributing to and managing the report writing or liaising with the medical writing/narrative group to ensure report is completed according to current requirement. Responsible for report publication.
* In collaboration with the Medical Expert and CTT, coordinate the ongoing medical / scientific review of the clinical trial data (as needed), and coordinate the data analysis and interpretation including the development of first interpretable results, the clinical study report, publications and internal/external presentations. May support the Medical Expert on project documentation e.g. Briefing books, IBs, Annual Safety Reports, responses to Health Authority questions, etc.
Education:
BSc or MSc in life sciences or nursing; PhD level scientist with life sciences background; PharmD or equivalent qualification or work experience.
Relevant experience (5+ years) in clinical trial management (e.g. study management in a multi- national environment using different models for trial execution).
Demonstrated leadership and problem-solving skills.
rack record of managing multiple, complex clinical trials.
Capable of clear written and verbal expression of ideas, an active/proactive communicator.
Ability to interact with a wide range of people and build strong positive relationships.
Potential for customer orientation awareness and focus.
Computer literacy.
Excellent organizational skills and interpersonal skills.
Ability to work independently and in a team environment managing multiple priorities.
Michael Bailey International is acting as an Employment Business in relation to this vacancy.