- Merck & Co. (Rahway, NJ)
- …with talented and dedicated colleagues while developing and expanding your career.-- Director (Principal Scientist ) has primary responsibility for the planning ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage...safety and efficacy as well as new drug applications, clinical study reports, or publicationParticipation in internal … more
- Merck & Co. (Rahway, NJ)
- …talented and dedicated colleagues while developing and expanding your career.The Senior Director (Sr. Principal Scientist ) has primary responsibility for the ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage...safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in internal… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Clinical Director (Principal Scientist ) has primary responsibility for planning and directing clinical research activities involving ... in Immunology. With a focus on late-stage development, the Clinical Director will manage the entire cycle...safety and efficacy as well as new drug applications, clinical study reports, or publication;Participation in internal … more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical ... Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle...safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in internal… more
- Merck & Co. (Rahway, NJ)
- …role of Associate Director . The team is part of the Global Clinical Development organization and has oversight over drug development aspects related to ... Job DescriptionWe are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics...clinical pharmacology and pharmacometrics of oncology drugs from post-PCC… more
- Merck & Co. (Rahway, NJ)
- …the role of Director . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical ... and Responsibilities: - We are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics -...of drug development. As a subject matter expert, the Director within the QP2-IO Group will work closely with… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. ... documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. ... documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical … more
- Bristol Myers Squibb (Summit, NJ)
- …pioneer. Join us and make a difference. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine, the TM Sr. Principal Scientist will be ... group. The individual will be responsible for TM and clinical biomarker activities to support drug development programs in...and analysis and associated timelines by working with relevant internal functions and CROs; + Prepares and delivers … more
- Merck (Rahway, NJ)
- …and dedicated colleagues while developing and expanding your career. The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning ... Our company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of… more
- Merck (Rahway, NJ)
- …with talented and dedicated colleagues while developing and expanding your career. Director (Principal Scientist ) has primary responsibility for the planning and ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage...clinical study reports, or publication + Participation in internal and joint internal /external research project teams… more
- Merck (Rahway, NJ)
- **Job Description** **Position Description:** **Associate Principal Scientist , Outcomes Research** Under the guidance of a senior leader, an Associate Principal ... Scientist has primary responsibility for planning/managing real world and...strategies and outcomes research activities, while considering insights from internal and external stakeholders. + In collaboration with … more
- Merck (Rahway, NJ)
- …execution of clinical protocol(s). This may include: + Serving as the lead clinical scientist on a clinical trial team. + Leading medical monitoring ... clinical data/medical protocol deviations in collaborations with the Clinical Director . **Other responsibilities include:** + Collaborating cross-functionally… more
- Ascendis Pharma (New York, NY)
- …to grow and develop their skills. We are looking for a Regional Medical Scientist (RMS) who is the external facing scientific expert in Medical Affairs at Ascendis ... Pharma that communicates confidently about our products using clinical and scientific expertise. The RMS is responsible for...FDA. The position is remote and reports to the Director , Field Medical Team. Key Responsibilities + Serve as… more
- Organon & Co. (Jersey City, NJ)
- …Director in Organon Regulatory CMC New Products, the Associate Principal Scientist (Associate Director ) is responsible for Regulatory Chemistry Manufacturing ... & Controls (CMC) aspects of clinical phase through market product registration for the assigned...development products and commercially approved compounds. The Associate Principal Scientist may also support project team goals and organizational… more
- New York University (New York, NY)
- …by Design (http://www.rebuildbydesign.org/) is looking for an Assistant Research Scientist /Assistant Project Manager to join our dedicated and energetic team. ... communities to understand their risks better. Position The Assistant Research Scientist /Assistant Project Manager will address community needs by working with… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …(edaravone) oral suspension in 2022. The company handles research, clinical development, sales, marketing, medical affairs, supply chain,and business development ... working closely with Drug Safety Global Safety Team (GST) Chair (Medical Director ). The Manager, Drug Safety will perform signal management process activities for… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- … to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution ... scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads...may include the following: + May function as lead Clinical Scientist for program, and/or as delegate… more
- Merck (Rahway, NJ)
- **Job Description** The **Senior Clinical Director (Sr. Principal Scientist )** has primary responsibility for the strategic planning and directing ... Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle... study reports, or publication; and + Participation in internal and joint internal /external research project teams… more
- AbbVie (Branchburg, NJ)
- …(IEST) lead, Clinical Program Lead and Clinical Science Lead and Clinical Scientist . The Associate Director , Clinical Development should expect ... (eg, Regulatory documents, presentations at congresses and publications). + As the Clinical Scientist , be responsible and accountable for the scientific/… more
