- 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
- Merck & Co. (North Wales, PA)
- Job DescriptionPosition Description: Associate Principal Scientist , Outcomes Research Under the guidance of a senior leader, an Associate Principal Scientist has ... evidence strategies and outcomes research activities, while considering insights from internal and external stakeholders.In collaboration with internal teams and… more
- Merck & Co. (North Wales, PA)
- …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 in the… more
- 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. (North Wales, PA)
- …with talented and dedicated colleagues while developing and expanding your career.The Clinical Director (Principal Scientist ) has primary responsibility for ... 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; andParticipating 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
- Bristol Myers Squibb (Princeton, NJ)
- … Clinical Trial Lead or Co-Lead as needed + May represent the Clinical Scientist function in various process improvement initiatives and/or cross functional ... internal and external collaborators independently and oversee collaboration between clinical scientist and external partners for scientific advice + Lead… more
- United Therapeutics (Durham, NC)
- …as required **For this role you will need** Minimum Requirements + For Senior ( Clinical ) Product Development Scientist level: + Bachelor's degree with at least ... to summarize the methods and results; Work with other internal functional areas (eg, Regulatory, Safety, Data Management) to... clinical development with a PhD/PharmD + For ( Clinical ) Product Development Associate Director level: +… more
- BeiGene (San Mateo, CA)
- **General Description:** _The Director , Safety Scientist supports assigned compounds in conjunction with Product Safety Leads (PSLs) and leverages clinical ... + Responsible for effective execution, communication and influence with internal stakeholders (eg, clinical development, medical, regulatory, labeling)… 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
- BeiGene (Emeryville, CA)
- **General Description:** _The Associate Director , Safety Scientist supports assigned compounds in conjunction with Product Safety Leads (PSLs) and leverages ... + Contribute to effective execution, communication and influence with internal stakeholders (eg, clinical development, medical, regulatory, labeling)… more
- MicroVention, Inc. (Aliso Viejo, CA)
- …Take a closer look at what MicroVention(R) TERUMO has to offer. The Sr. Clinical Scientist provides scientific expertise for developing clinical evaluations, ... trial registrations and results postings and scientific publications. The Sr. Clinical Scientist position will drive scientific activities associated with the… more
- Bristol Myers Squibb (Princeton, 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
- AbbVie (Irvine, CA)
- …Aesthetics on LinkedIn. The Neurotoxin Research Group at AbbVie seeks an accomplished scientist and leader. The Director /Senior Principal Research Scientist ... desired pharmacological characteristics * Liaise with toxicology, immunology, bioanalytical, clinical development, and commercial colleagues * As programs advance,… more
- AbbVie (Irvine, CA)
- …and senior leadership. Responsibilities: In collaboration with a Therapeutic Area Scientific Director (TA-SD), the Clinical Scientist and/or Clinical ... global or regional responsibilities and fulfill the role of Clinical Scientist and/or Clinical Science...II should expect to be asked to participate in internal process improvement activities within R&D and Clinical… 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
