Clinical Scientist, Neuropsychiatry

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Janssen Research & Development, L.L.C., a division of Johnson & Johnson’s Family of Companies, is recruiting a Clinical Scientist, Neuroscience located in one of our Janssen Hubs (prefered locations are: Beerse (Belgium), Basel (Switzerland) or New Jersey (US)). At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at www.janssen.com and follow us @JanssenGlobal. The Clinical Scientist is a responsible member of a clinical team dedicated to the development and execution of clinical strategies and the clinical and operational implementation of a compound program in mood disorders. In this role, you will provide active scientific contribution to a cross-functional clinical team developing a molecular entity. You provide input to the clinical development plan, work on the development of the clinical trial protocol, clinical trial materials, and take responsibility for coordinating completion of clinical study reports and supports preparation of relevant documents for regulatory filings. This role involves extensive team matrix interactions with colleagues from a number of different disciplines. You may be asked to contribute to the evaluation of scientific opportunities in the therapeutic area Key Areas Of Responsibilities: Participates in preparation of clinical development plans, trial protocols, has direct responsibility for trial set up and monitoring and takes responsibility for completion of clinical study reports Assists Physicians in evaluation of adverse events (pre and post-marketing) for relationship to treatment. Safety assessments are the responsibility of the project physicians (PP) Assists Regulatory Affairs in determining requirements for any corrective actions or health authority reporting Interprets, reports and prepares oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissions Close interactions with Project Physicians and Physicians across programs Other tasks and responsibilities: Assists Regulatory Affairs in the development of drug regulatory strategies Helps explore and evaluate new product ideas to assist in identifying new market opportunities Support general Clinical/Medical Affairs activities involving product evaluation, labeling and surveillance Participate on and may lead cross-functional teams for evaluation of new product ideas, implement franchise business strategies, etc. Reviews medical literature and related new technologies May be asked to assess medical publications emerging from the Team and its affiliates May be responsible, with appropriate colleagues, for review of Company advertising and promotional materials. Qualifications Master’s degree in a relevant field (biomedical Sc, Biology, PharmD, …) or equivalent by experience with proven track record Min 3-5 yrs. experience in clinical research, Drug Development or pharmaceutical industry (clinical research) experience Experience working in a Matrix environment Energy and passion are essential Familiarity with key clinical research tasks, including protocol authorship; trial execution; case report form design; data management and report writing Proficient in English: Good oral, written, and presentation skills Good sense of cultural sensitivity and diversity. Demonstrated ability to manage multiple, diversified tasks concurrently and to prioritize tasks effectively Strong project management skills. An ability to handle complex projects and to overcome delays and obstacles Good team member and interpersonal skills. The ability to advise, persuade and negotiate with colleagues and external parties in a supportive and encouraging fashion Are you ready to make an impact? If you want to leave your personal mark and be valued for who you are, Johnson & Johnson offers an unusual experience to professionals looking for an opportunity to work with hardworking people who share your real passion for caring in an environment that empowers you to drive your own career and that you feel you can bring your whole self to work. We provide you an environment to fulfil your career aspirations as well as promoting your physical and mental wellbeing. You will receive a competitive compensation and benefits package as well as benefits that can be tailored to what is valuable to you throughout different stages of your life. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Ready for your next breakthrough? Apply now. We want YOU! Primary Location Belgium-Antwerp-Beerse- Other Locations Europe/Middle East/Africa-Switzerland-Basel-City-Basel Organization Janssen Pharmaceutica N.V. (7555) Job Function R&D Requisition ID 2206002091W