- Bristol Myers Squibb (Princeton, NJ)
- …careers.bms.com/working-with-us . **Position Summary** This Director, Medical Evidence Generation (MEG) Clinical Trial Physician (CTP) - Cell Therapy (CT) role ... MD required (or x-US equivalent) plus 2-3 years of clinical trial experience, either in industry or...experience, either in industry or academic setting; expertise in drug development process and clinical research; experience… more
- Bristol Myers Squibb (Princeton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Clinical Trial Physician sits within Clinical Development, which is ... of expertise in key Health Authority interactions and advisory board meetings as Senior Clinical Trial Physician + Authors/drafts clinical content for CSRs,… more
- Sumitomo Pharma (Trenton, NJ)
- …rigorous and innovative trial protocols. + Oversee clinical trial execution, ensuring quality, patient safety , and compliance with GCP standards. ... to the end of the product's life cycle. + Clinical Trial Oversight: Develop and oversee ...clinical and medical expertise across all stages of drug development, from preclinical transition to post-marketing. + Stay… more
- University of Pennsylvania (Philadelphia, PA)
- …vigilance in patient safety , protocol compliance and data quality. + Communicate clinical trial patient activity to the investigational drug pharmacy ... research performed. He/she will be responsible for all aspects of clinical trial coordination including subject recruitment, detailed data entry, subject… more
- Bristol Myers Squibb (Princeton, NJ)
- …Summary / Objective** + Responsible for implementation, planning, and execution of assigned clinical trial activities. Serves as Clinical Trial ... team members + May support clinical development planning (collaboration with Clinical Development Lead/ Clinical Trial Physician for provision and… more
- University of Pennsylvania (Philadelphia, PA)
- …vigilance in patient safety , protocol compliance and data quality. + Communicate clinical trial patient activity to the investigational drug pharmacy ... accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and...and ensure adherence to protocol. Show vigilance in patient safety , protocol compliance and data quality. Ensure drug… more
- Bristol Myers Squibb (Princeton, NJ)
- …Summary / Objective** + Responsible for implementation, planning, and execution of assigned clinical trial activities. + Successfully leads, plans, and executes ... presentation at SIV and Investigator meetings and support on Study committee (eg, safety review) activities. + Author/review clinical study reports (CSRs) and … more
- Bristol Myers Squibb (Princeton, NJ)
- …projects + Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects + ... and develop productive relationships with external vendors + Sound knowledge of Clinical Drug Development Process, FDA/ICH guidelines and industry standard… more
- Bristol Myers Squibb (Princeton, NJ)
- … development projects. Plan, coordinate and deliver complete, high quality and reliable clinical trial data. Responsible for end-to-end clinical data ... related work experience. Must have experience with/in: + Medidata RAVE; + Clinical Drug Development Process, FDA/ICH guidelines and industry standard practices… more
- Catalent Pharma Solutions (Philadelphia, PA)
- …Demand Led and Decentralised Trial Supply are two of the most exciting clinical trial supply innovations in recent times. Catalent is at the forefront of ... through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.** **The...+ Thorough knowledge of GMP + Good knowledge of drug development process and GCP requirements in clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Nurse C/D (Abramson Cancer Center) Job Profile Title Clinical ... is a world leader in developing and conducting innovative clinical trials for the prevention, diagnosis, and treatment of...outcomes, and offer the best available innovative care to trial participants. The ACC CRU is instrumental in the… more
- Bristol Myers Squibb (Princeton, NJ)
- …Articulating clinical development strategy + Analyzing, interpreting, and acting on clinical trial data to support development + Serving as principal ... and interpretation of studies to select the most promising drug candidates for later development. + Serves as a...Clinical Scientist for medical questions and education (including safety management guidelines) + Assesses key safety -related… more
- University of Pennsylvania (Philadelphia, PA)
- …and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A (Department of Endocrinology, Diabetes and Metabolism) Job ... Profile Title Clinical Research Coordinator A Job Description Summary This entry-level...regulatory knowledge with the duty to protect research patient safety and data integrity. This position will report administratively… more
- University of Pennsylvania (Philadelphia, PA)
- …with Investigational New Drug (IND), Investigational Device (IDE) and Clinical Trial Agreement (CTA) exemption determinations. + Program Leadership: Provide ... annual reports, source docs, training slides, manuel of procedures (MOPs), Data Safety Monitoring Board (DSMB) charter, Clinical Report Forms (CRFs), standard… more
- Bristol Myers Squibb (Princeton, NJ)
- …development / management + Pharma R&D experience, preferably Clin Dev't, Trial Operations, Biostatistics, Regulatory, Safety , etc + Transformational change ... strategic initiatives. **Position Summary** Support the development and execution of Drug Development's (DD) Innovation strategy in partnership with DD Leaders,… more
- Highmark Health (Trenton, NJ)
- …& Therapeutics Committee (35%): + Pre-work and Preparation: + Review and analyze drug formulary proposals, clinical trial data, and relevant literature. ... Pharmacology & Therapeutics Committee and serves as a Medication Safety Champion. Reviews drug proposals, chairs meetings...degree. + 10 years of extensive experience in medication safety and clinical pharmacology. **Preferred** + None… more
- Merck (North Wales, PA)
- …or related field and at least 5 years SAS programming experience in a clinical trial environment or + MS in Computer Science, Statistics, Applied Mathematics, ... related field and at least 3 years SAS programming experience in a clinical trial environment. **Required Skills:** + Effective interpersonal skills and ability… more
- Merck (North Wales, PA)
- …Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. + MS in Computer Science, Statistics, Applied Mathematics, ... related field plus 7 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** + Excellent… more
- J&J Family of Companies (Spring House, PA)
- …the clinical study of immunologic disease, immunologic pathways, and in early clinical trial design and execution. TS has expertise in biomarker development, ... for humanity. Learn more at https://www.jnj.com **Job Function:** Discovery & Pre- Clinical / Clinical Development **Job Sub** **Function:** Clinical … more
- Bristol Myers Squibb (Princeton, NJ)
- …is a plus); within Drug Development ( Clinical Development, Trial Operations, Biostatistics, Regulatory, Safety , Project Management, etc.) + Demonstrated ... cross-functional Business Process Owners (eg Biostatistics, Regulatory, Clinical Development, Safety and Clinical Trial operations). This position will… more