At Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress. That’s why for more than 130 years, we have aimed to keep people well at every age and every stage of life. Today, as the world’s largest and most broadly based healthcare company, we are committed to using our reach and size for good. We strive to improve access and affordability, create healthier communities, and put a healthy mind, body and environment within reach of everyone, everywhere.
Every day, our more than 130,000 employees across the world are blending heart, science and ingenuity to profoundly change the trajectory of health for humanity.
We are recruiting to fill the position of:
Job Title: Associate Director, Clinical Research
Req ID: 2105927559W
- 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 complex compound program.
- The Clinical Scientist provides active scientific contribution to a cross-functional clinical team developing a molecular entity.
- The Clinical Scientist provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and takes 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.
- The Clinical Scientist may be asked to contribute to the evaluation of scientific opportunities in the therapeutic area.
- 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 Responsibilities / Detailed Duties:
- Assists Regulatory Affairs in the development of drug regulatory strategies
- 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
- 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
- May be responsible, with appropriate colleagues, for review of Company advertising and promotional materials.
For this Associate Director function we are looking for:
- Master’s Degree or PhD with 10-plus years of experience in research & development in low- and middle-income countries, including 5-plus years of drug development with strong logistical & medical supply expertise. This position will provide cross program advise to the GPH Clinical Scientists in the Capacity Development Group, on logistical and medical supply risks and challenges in low- and middle-income countries.
- Experience with vaccine programs is an asset.
- Living in, or willing to live in a Sub-Saharan African country is an asset.
How to Apply
Interested and qualified candidates should:
Click here to apply online