- WuXi AppTec (Plainsboro, NJ)
- **Overview** The Clinical Research Associate III Senior Oncology performs and coordinates aspects of field-based and office-based monitoring and data quality ... **Essential Job Functions:** + Responsible for all aspects of clinical monitoring and required reporting, including pre- study ...or supervisor, including but not limited to mentoring of Clinical Research Associate (CRA) I and II… more
- Bristol Myers Squibb (Princeton, NJ)
- …integrity & completeness of all data types (eCRF and non eCRF) collected in BMS clinical trials from study start to database Lock . **Position Summary:** The ... Senior Manager, Clinical Data Management is a...R&D pipeline . This role may report into Director, Clinical Data Management or Associate Director, … more
- Merck (North Wales, PA)
- …Finance** Under the guidance of the Oncology Clinical Development Finance Associate Director, the Finance Senior Specialist will: + Provide financial ... ** Senior Specialist, Oncology Clinical Development...as well as provide financial support related to assigned clinical studies + Be the primary point of… more
- Merck (West Point, PA)
- …Writing & Communications** Responsible for authoring of clinical protocols, clinical investigator brochures, clinical study reports, regulatory agency ... ongoing trials to identify and mitigate patient, study design, data or study conduct issues. Reviews and interprets clinical trial data. May conduct on-site… more
- Merck (North Wales, PA)
- …of clinical biomarker specimen collection, testing and data delivery activities in clinical studies . The primary focus of this position is in oncology, ... efficient delivery of the biomarker operational aspects of each study . This position will report into the Associate...as a co-author for drafting relevant biomarker sections of clinical study protocol + Work closely with… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . ** Sr . Principal Scientist DMPK Project Representative** Challenging. Meaningful. Life-changing. ... and PK (pharmacokinetics) support for all pipeline assets throughout clinical development, from candidate nomination through registration and lifecycle management.… more
- Merck (North Wales, PA)
- …with talented and dedicated colleagues while developing and expanding your career. The Senior Clinical Director ( Sr . Principal Scientist) has primary ... Senior Director will manage the entire cycle of clinical development, including: study design, placement, monitoring,...of Clinical Scientists in the execution of clinical studies + Work closely with a… more
- WCG Clinical (Princeton, NJ)
- Senior Associate , Operations QA & Compliance (Remote) **General Information** **Location:** Princeton, NJ, Remote **Organization:** WCG **Job Type:** Full Time - ... to $97,000 GPS level: P3 **JOB SUMMARY** : The Senior Associate , Operations QA & Compliance is...current regulatory and GCP guidelines as they apply to clinical studies and WCG services/products. + Strong… more
- J&J Family of Companies (Horsham, PA)
- …issues. * Write, as well as provide editorial comments, for phase IIIb/IV clinical study reports, abstracts and manuscripts related to J&J Innovative Medicine ... Associate Medical Director, Rheumatology Therapeutic Area - Medical...least 3-5 years of total work experience required * Clinical study , registry, or real-word evidence … more
- Novo Nordisk (Plainsboro, NJ)
- …with Novo Nordisk policies and procedures. Relationships This position reports to a Senior Director within the Clinical Data Science & Evidence (CDSE) - ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...you ready to make a difference? The Position The Associate Director, Research Partnerships (RP) is responsible for developing… more
- Intermountain Health (Trenton, NJ)
- …knowledge and improve ROI of risk adjustment activities. We will hire at Senior or Staff level depending on qualifications. (see details below) Unfortunately, we are ... this position. We apologize for the inconvenience. **Essential Responsibilities/Accountabilities:** Associate : . Maintains current knowledge of risk adjustment models… more
- Bristol Myers Squibb (Princeton, NJ)
- …the conduct of reviews, development, and execution of medical evidence generation studies for Cardiovascular as well as be responsible for driving cross-therapeutic ... team to maximize the effectiveness of the review of new, evidence generation studies , including ISRs + Oversee tracking and measurement of performance for medical… more
- Kelly Services (Lawrenceville, NJ)
- Kelly is hiring for an ** Associate Research Scientist** position with one of our clients in **Lawrenceville, NJ.** + Full time- W2 + 6 months contract (May be ... programs as they transition from discovery to a FIH study . The qualified candidate will be responsible for running...responsible for running various experiments under the guidance of senior scientists. The type of experiment will vary, depending… more
- Integra LifeSciences (Princeton, NJ)
- …extensions and/or line trimming, forecasting, pricing strategies, labeling revisions, clinical studies , manufacturing and customer service/operations support for ... help improve outcomes. **SUPERVISION RECEIVED** Under direct supervision of Associate Director, Global Marketing - Surgical Reconstruction, TT **SUPERVISION… more
- Cline Davis & Mann (Doylestown, PA)
- …tracking studies , demand, conjoint, segmentation) with limited overview by senior staff + Strong analytic and communication skills, including superior writing ... you do, we definitely want to speak with you! **Ti** **tle:** Associate Director, Quantitative Market Research **Department/Discipline:** Research We are looking for… more
- Bristol Myers Squibb (Princeton, NJ)
- …. Position Summary The Finance Resource Management role is an Associate Director role that collaborates with Global Program Teams (GPT) and ... other support functions. The Associate Director serves as the day-to-day contact for all...business cases, cost plans and financial insights to assist senior leadership in making sound investment decisions + Support… more
- Novo Nordisk (Princeton, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... a living. Are you ready to make a difference? The Position The Associate Director, Regulatory Affairs - Advertising & Promotion will provide strategic regulatory… more
- Novo Nordisk (Princeton, NJ)
- …of all clinical and nonclinical documents for submissions, eg, clinical protocols and study reports, preclinical reports, investigator brochures, application ... MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D… more
- Novo Nordisk (Plainsboro, NJ)
- …for aligned therapeutic / franchise area(s). Relationships + Reports to the Senior Director of Value Communication and Contracting Strategy + Interacts frequently in ... collaboration with internal management and senior level global stakeholders + Interacts internally with Strategic...strategy for all pipeline products starting in Phase II clinical trials. Generates insights to support G3 decision-making for… more
- Novo Nordisk (Princeton, NJ)
- …goals, including those specifically aligned with the planning & successful delivery of studies within the clinical trial portfolio. Assists in creating, leading ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the… more