- Merck & Co. (North Wales, PA)
- …the necessary processes to ensure high quality individual case and aggregate safety reporting. Interpret PV regulations related to drugs, vaccines, biologics, and ... with all of company's business units to ensure compliance and patient safety .Assist in the development and leadership of team members.Develop and implement… more
- Merck & Co. (North Wales, PA)
- …drugs;-Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical ... statistics, and manufacturing to manage clinical development projects; andAssist the Senior Director , Executive Director , and/or Associate Vice President in… more
- Merck & Co. (North Wales, PA)
- …and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical ... Job DescriptionThe Associate Vice President (AVP) has primary responsibility for...of generating early clinical development plan and Investigational New Drug applicationsDeveloping clinical development strategies for investigational or marketed… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …internal and external stakeholders. Relationships This position will report to Senior Director Safety Surveillance, US East Coast Development Hub. Key internal ... DMCs, and Academia. Line management of Senior Global Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist(s)/ Associate within Safety … more
- Merck (North Wales, PA)
- …the necessary processes to ensure high quality individual case and aggregate safety reporting. Interpret PV regulations related to drugs, vaccines, biologics, and ... of company's business units to ensure compliance and patient safety . + Assist in the development and leadership of...the business to implement system improvements and updates of safety database. + Provide expert guidance on policies and… more
- Merck (West Point, PA)
- …Our Company is seeking a highly motivated candidate for the position of Director , Vaccine Drug Product Development. Vaccine Drug Product Development ... The Director will report to the Executive Director of Vaccine Drug Product Development, have...be responsible for a team of 10-20 senior and associate level scientists. The incumbent will be responsible for… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …is true to the best of my knowledge. **Job Description** ** Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Gastrointestinal ... vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing...Regulatory Operations, Drug Discovery Units, DMPK&M, and Drug Safety Research and Evaluation) to recognize… more
- Somerset County YMCA (Somerville, NJ)
- …dedication of our gymnasts and coaches. Somerset Valley YMCA is seeking an Associate Program Director of Gymnastics to provide direct leadership and development ... gymnast, or both. POSITION PURPOSE Under the direction of the Wellness & Sports Director and Associate Branch Executive Director , this role will have… more
- Sunrise Senior Living (Newtown Square, PA)
- …**COMMUNITY NAME** Sunrise of Newtown Square **Job ID** 2024-216350 **JOB OVERVIEW** The Associate Director of Sales (ADOS) is responsible for supporting and ... duties the ADOS may, under the supervision of the Director of Sales (DOS), Director of Sales...promoting Risk Management programs and policies and adhering to safety rules and regulations. + Practices safety … more
- Ascendis Pharma (Princeton, NJ)
- …for employees to grow and develop their skills. The Regulatory Affairs (RA) Associate Director , Labeling will be responsible for labeling activities across ... of Patients, Science, and Passion, we use our TransCon(R) drug development platform to fulfill our mission of developing...Americas and supporting global needs as required. The RA Associate Director , Labeling will be overall responsible… more
- Bausch Health (Bridgewater, NJ)
- …and values drive our collective progress and impact. The Associate Director , Advertising and Promotion, Prescription Drug Products, reviews, approves and ... violative competitive materials for forwarding to the FDA Office of Prescription Drug Promotion (OPDP) or Advertising and Promotion Labeling Branch (APLB) as… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for ... of labeling content and strategy of multiple assigned products in various stages of drug development, which may include one high complexity product and updates to or… more
- BeiGene (Hopewell, NJ)
- **_General Description:_** The Associate Director Site Technical Services is responsible for the day-to-day activities of the Validation team, Metrology, CMMS ... authors and works with CQV validation of start-up Green-Field Project. Works with Drug substance, Drug Product, QC, and Warehouse areas to support validation… more
- Bristol Myers Squibb (Princeton, NJ)
- …every treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director , Biostatistics is a core member of cross-functional development ... on protocol teams as a scientific partner in the drug development process. + Ability to present summary data...engagement, and enhances the Company culture. To protect the safety of our workforce, customers, patients and communities, the… more
- Bristol Myers Squibb (Princeton, NJ)
- …**,** the ideal candidate: + Is responsible for the oversight of the nonclinical safety -evaluation programs for selected drug candidates. + Assists in the proper ... Read more: careers.bms.com/working-with-us . This is a Hybrid role Nonclinical Safety (NCS), within Nonclinical Research and Biotherapeutics, is responsible for… more
- Novo Nordisk (Plainsboro, NJ)
- …internal and external stakeholders. Relationships This position will report to Senior Director Safety Surveillance, US East Coast Development Hub. Key internal ... DMCs, and Academia. Line management of Senior Global Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist(s)/ Associate within Safety … more
- BeiGene (Hopewell, NJ)
- …activities are performed in accordance with GMP, company SOPs and Health and Safety policies. + Manage all method transfer and method validation activities for ... chemistry or related). + Minimum of 10 years' experience in biological drug product quality control in an FDA-regulated biotechnology, pharmaceutical company with… more
- Bristol Myers Squibb (Princeton, NJ)
- …science, clinical research, or equivalent + Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations + Proficient ... KOLs, indication(s), compound(s) under study (including MOA, PK/PD, biomarker & safety profile) + Proficient critical thinking, problem solving, decision making… more
- Gentiva (Hamilton, NJ)
- …lives every day. **Overview** We have an exciting and rewarding opening for an **Executive Director - RN** to join our team in Hamilton Township NJ! Join us and find ... everything we do, day in and day out. **Executive Director Responsibilities:** As an **Executive Director RN**...You** + Education: + Registered Nurse with minimum of Associate 's Degree in Nursing required + Bachelor's degree in… more
- Merck (North Wales, PA)
- …Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study ... and manufacturing to manage clinical development projects; and + Assist the Senior Director , Executive Director , and/or Associate Vice President in ensuring… more
