What are the responsibilities and job description for the EXECUTIVE DIRECTOR position at Easyhiring?
We are a recruiting company EasyHiring looking for candidates for the position of Executive Director in Hillsborough, NJ for our partners
Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at us is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
We recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.
Position: Executive Director, Development Drug Metabolism and Pharmacokinetics (DMPK)
Job Description
The Executive Director, Development Drug Metabolism and Pharmacokinetics (DMPK) oversees the research and regulatory activities within the Development DMPK team. The role encompasses scientific and administrative leadership of the entire development portfolio at BMS, including all drug modalities, from pre-IND status to regulatory approval. The successful candidate will be responsible for representing the team at internal governance meetings, advising on the best approaches for regulatory reviews and program progression, and ensuring appropriate compliance with guidelines across all health authorities for all matters relating to Development DMPK. The successful candidate will report to the head of Pharmaceutical Candidate Optimization (PCO) and interface with scientists focused on Discovery efforts, collaborate with colleagues in Clinical Pharmacology and Pharmacometrics, and work with leaders in Non-Clinical Safety, Bioanalytical and CMC functions to enable successful drug approval. The PCO organization is a multi-disciplinary department whose cross-functional teams apply deep expertise in DMPK, toxicology, pharmaceutics and bioanalysis to identify and solve issues, discover high quality drug candidates and enable their clinical development.
Key Responsibilities
- Lead research efforts and overall effectiveness of the Development DMPK group, consisting of approximately 25 people, including Ph.D. scientists and research associates (BS or MS training), with some scientists working in locations other than Lawrenceville, NJ.
- Provide strategic direction, development and implementation of work efforts within the group and managing resources within the group to meet the department goals.
- Ensure effective regulatory progression of development candidates by engaging directly with regulatory authorities and/or providing guidance for regulatory discussions across the DMPK team.
- Represent Development DMPK in strategic meetings and discussions across Development project teams and with Global Drug Development leadership
- Oversee the review and approval for all regulatory documents (IND, NDA, BLA, MAA, etc) prepared by the Development DMPK team.
- Interface with the early development teams and Clinical Pharmacology to ensure effective engagement and timely study conduct for entire portfolio; interface with scientists in PCO and non-clinical safety to coordinate effective DMPK data packages for IND submissions.
- Demonstrate leadership consistent with the BMS’s philosophy, including attracting and retaining top key talent critical to business success, developing team members to support the BMS portfolio including identification of new skills and approaches to DMPK research.
Education/Experience
- Ph.D. degree in any area of drug disposition, with emphasis on metabolism, pharmacokinetics or biochemical toxicology, with experience in drug discovery and development.
- At least 15 years of experience in conducting and leading research efforts in drug metabolism and pharmacokinetics; preference to scientists who are familiar with advancing candidates through development, with knowledge of regulatory requirements for all DMPK issues and a proven track record of effective interactions with health authorities.
- Outstanding problem-solving skills, with proven ability to integrate across disciplines to address issues and identify mitigation strategies.
- Highly effective written and oral communication skills including contributions to the published literature, and a track record of successful regulatory submissions.
- Strong interpersonal skills with evidence for effective management of a dynamic team and commitment to professional development of all personnel.
If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibilityto access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Job Type: Full-time
Work Location: On the road