Director of Regulatory Strategy and Clinical Excellence
Kaye/Bassman International
Kaye/Bassman International is seeking a Director responsible for driving regulatory projects that align with company objectives in Parsippany-Troy Hills, New Jersey. This role involves shaping regulatory strategies for various programs and ensuring integration into the overall strategy. The ideal candidate will have over 10 years of regulatory affairs experience, lead interactions with Health Authorities, and possess exceptional communication and project management skills. This position will play a critical role in navigating complex regulatory landscapes and influencing key decisions. #J-18808-Ljbffr Kaye/Bassman International
- Position: The Director will direct, manage, and implement regulatory projects in support of company goals across clinical strategy areas. The position plays a major role in shaping a cohesive... ...at all levels of the organization. Excellent analytical, critical thinking,...SuggestedLocal area
$203k - $267k
...directs, manages, evaluates and implements regulatory projects in support of company goals in the area of clinical strategy. The position will play a major role in shaping... ..., programs, and initiatives Demonstrates excellent communication skills with ability to impact...SuggestedFor contractorsLocal areaFlexible hours- Kaye/Bassman International is leading a search for a Senior Director, Global Regulatory Clinical Strategy. This role focuses on overseeing global regulatory strategies across various clinical and non-clinical programs. The ideal candidate will have 15+ years of experience...Suggested
- I am leading a search for a Senior Director, Global Regulatory Clinical Strategy at a commercial-stage biopharmaceutical organization focused on non-opioid pain management and regenerative health solutions, with a robust pipeline spanning small molecules, biologics, and...Suggested
- Bristol Myers Squibb EU Policy is seeking a Director of Biostatistics in Madison, New Jersey.... ...field with significant experience in clinical trials and drug development. Strong... ...R, and Python are required, along with excellent organizational and communication abilities...Suggested
- Pacira BioSciences, Inc. seeks a regulatory affairs leader to manage complex projects and guide strategic decisions. With a focus on non-opioid pain management, you will oversee regulatory submissions and collaborate cross-functionally. The ideal candidate has 10+ years...Flexible hours
- Ferring Pharmaceuticals Inc. is looking for a Director, Field Excellence and Operations in Parsippany, NJ. This position drives Sales Force Effectiveness and field strategy, requiring strong leadership and analytical skills. Candidates should have over 12 years of experience...Remote work
- Job Title Manager, Clinical Data Standards Location Basking Ridge, NJ 07920 Duration Contract till Nov 2026 with possibility to extend... ...standards, expertise in Study Data Tabulation Model (SDTM), excellent verbal/written skills, analytical, and interpersonal skills...Contract workWork experience placementLocal area
- Jobsbl in Parsippany, NJ is seeking a Manager of Scientific Affairs to oversee clinical studies and ensure compliance with regulatory standards. This hybrid role requires strong leadership skills and a deep understanding of clinical practices. The ideal candidate will...
- Allergan in Florham Park, NJ, is seeking a Medical Director to manage clinical trials and lead cross-functional teams. Responsibilities include... ...mentorship programs, and ensuring compliance with regulatory standards. The ideal candidate has an M.D. degree, significant...
$165.5k - $214.17k
...lives of patients for generations to come. Clinical Operations is responsible for the... ...applicable SOPs, company policies and regulatory guidelines to provide timely and high‑quality... ...risk assessment and mitigation strategies. Resolves issues as needed within national...Contract workFor contractorsLocal areaWorldwide- ...offering contingent labor as a variable cost. Job Description The Clinical Program Manager will work cross functionally to develop, track... ...project, planisware, or similar project management systems and excel. Candidate must possess strong communication skills, both oral...For contractorsWork at officeImmediate start
- ...teams. Accountable for HEOR strategies and execution, looks to shape... ...meets ethical, scientific, regulatory, commercial, and quality requirements... ...and communication excellence of all data elements agreed... ...leading complex products and/or clinical development in support of...Full timeWork experience placement
$260k - $295k
Overview Join to apply for the Senior Director, Global Commercial Strategy role at Shionogi Inc. (U.S.) .... .../reimbursement, health outcomes, clinical, regulatory, and project management.... ...and problem-solving capabilities. Excellent communication and presentation skills...Full timeWork at officeLocal area2 days per week3 days per week$285k - $315k
...Park, NJ, is seeking a Global Project Leader to provide strategic leadership for global clinical development programs in rare diseases. The role involves driving integrated strategies across the development lifecycle and ensuring successful delivery of program objectives...$169.68k - $254.52k
...and redefining ‘impossible’. Director, Regulatory Advertising and Promotion... ...shaping proactive regulatory strategies, driving regulatory... ...critically analyze and interpret clinical efficacy and safety data and... ...environment, demonstrating excellent written, verbal, and...Work at officeLocal area- In this position, the Regulatory Affairs CMC Director will lead the international Regulatory... ...regulatory registration strategies to support HUTCHMED’s... ...as a liaison between the clinical development teams and other... ...problem‑solving skills. Excellent written and oral communication...
$141.5k - $268.5k
...safety-net hospitals and clinics give better care to... ...implemented important strategies and policy changes to... ...profile340B Center of Excellence (COE)that brings together... ...and Innovation Director and is an expert in the... ...Monitor statutory and regulatory changes related to the...Full time- Daiichi Sankyo, Inc. is seeking a Senior Clinical Development leader to oversee global... ...across indications, ensuring alignment with regulatory expectations. You will provide senior... ...meetings and guide development and regulatory strategy, while ensuring CROs meet program goals....
- ...Inc. is seeking a full-time Asst. Program Coordinator in Parsippany-Troy Hills, NJ. This role involves coordinating and supervising clinical services and residential programming to support individuals in need. You will provide oversight to Behavioral Health Counselors...Full time
$65k
...seeking qualified individuals for a full-time role requiring clinical supervision in a dynamic team. This position offers a competitive... ...$70,000 for LPC/LCSW, alongside extensive benefits including excellent PTO, medical insurance, and ongoing professional development....Full time- ...Lab Inc. in Parsippany-Troy Hills, New Jersey, is looking for a full-time Assistant Program Coordinator to coordinate and supervise clinical services and residential programming. The role includes providing support to Behavioral Health Counselors and ensuring clinical...Full time
$119k - $150k
...evaluate and analyze data using a clinical focus. In addition,... ...Competency with MS Office, MS Excel, MS PowerPoint, and Tableau... ...Collaborate with the Magnet Program Director and other stakeholders to... ...Jersey, we advance innovative strategies in high-quality patient care,...Work experience placementLocal areaFlexible hoursShift workDay shiftAfternoon shift- ...Health in Paterson, New Jersey, is seeking a leader to direct clinical and administrative quality management activities across the organization... ...oversees patient safety and compliance with accreditation and regulatory standards. The ideal candidate holds a Master’s degree in...
- Daiichi Sankyo, Inc. is seeking an Executive Director for Oncology R&D, Global Clinical Lead, to oversee multi-program development and strategic regulatory submissions. The role drives clinical strategy, partners with CROs and senior management, and aligns development with...
- EmergencyMD is seeking a regulatory CMC specialist to provide global regulatory support throughout the product lifecycle in Morristown,... ...of relevant experience in the biotech or pharma industry, with excellent communication skills and the ability to interpret FDA...
$136.29k - $145.18k
...targets. Strong knowledge of MRP systems, planning and scheduling activities. Significant knowledge of LEAN manufacturing principles. Excellent verbal/written communication skills required for multi‑faced interactions with all levels of personnel within the organization, as...Work at officeLocal areaImmediate startFlexible hours$184.24k - $276.36k
Job Summary The Director, Regulatory Affairs Advertising and Promotion (RAAP) provides senior strategic... ...is responsible for leading regulatory strategy and decision‑making for complex, high‑... ..., Medical, Legal, Compliance, Clinical, Labeling, Public Affairs, Corporate Communications...Work at office- IQVIA is seeking an experienced professional to manage large, complex regulatory projects in Parsippany-Troy Hills, New Jersey. You will ensure quality deliverables are met on time and on budget, while providing strategic consultancy regarding regulatory processes. The...
- ...X and YouTube. Job Description The Director Regulatory Affairs Global Regulatory Lead (GRL II), Global Regulatory Strategy, is responsible for developing and implementing... ...life cycle of the product. Demonstrates excellent understanding of drug development and leadership...Full timeLocal areaWorldwide
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