- Merck & Co. (Rahway, NJ)
- …(GCP) studies, and occasionally Good Laboratory Practice (GLP) studies.The Associate Principal Scientist is the primary clinical study team leader ... Job DescriptionJOB DESCRIPTION SUMMARYThe Associate Principal Scientist is...primary function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the… more
- Merck & Co. (Rahway, NJ)
- …barriers to reimbursement and market access, and provide input into clinical , regulatory, payer/access, marketing and evidence generation strategies and programs.In ... Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers.Develop supplementary clinical data package in close partnership with markets and HTA statistics… more
- Merck & Co. (North Wales, PA)
- …other team members when opportunities arise. Primary Activities :Programmatically synthesize clinical / preclinical data into analysis ready structures from varied ... or related field plus 9 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences,… more
- Merck & Co. (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (North Wales, PA)
- …programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into ... at least 7 years SAS programming experience in a clinical trial environment OR a Bachelor's degree in Computer...field plus 9 years SAS programming experience in a clinical trial environment. Required Skills and Experience: Experience in… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving ... area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will… more
- Merck (Rahway, NJ)
- …(GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and ... **Job Description** **JOB DESCRIPTION SUMMARY** The Associate Principal Scientist is...primary function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the… more
- Astrix Technology (North Wales, PA)
- ** Associate Principal Scientist (Epidemiology)** Clinical North Wales, PA, US Pay Rate Low: 58.67 | Pay Rate High: 71.43 + Added - 14/04/2025 Apply for ... and innovative animal-health products, is in search of an Associate Principal Scientist to join...strategic plans in support of Early Development Teams (EDTs), Clinical Trial Teams (CTT) and/or Clinical Sub-teams… more
- Bristol Myers Squibb (Cambridge, MA)
- …track record of high-quality scientific publications in relevant fields For the Sr. Principal Scientist position, the starting compensation for this job is a ... the transition of drug candidates from early to late-stage clinical development, their approval and life cycle management. Early-stage...+ Minimum of 6 years post-PhD experience for Sr. Principal Level (and minimum of 8 years Post-PhD experience… more
- Merck (Rahway, NJ)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
- Merck (Rahway, NJ)
- …members when opportunities arise. **Primary Activities** **:** + Programmatically synthesize clinical / preclinical data into analysis ready structures from varied ... field plus 9 years SAS programming experience in a clinical trial environment + MS in Computer Science, Statistics,...7 or more years SAS programming experience in a clinical trial environment **Department Required Skills and Experience:** +… more
- Merck (North Wales, PA)
- …programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into ... at least 7 years SAS programming experience in a clinical trial environment OR a Bachelor's degree in Computer...field plus 9 years SAS programming experience in a clinical trial environment. **Required Skills and Experience:** + Experience… more
- Bristol Myers Squibb (Devens, MA)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position:** Principal Scientist , Manufacturing Technology (Process Transfer, Validation ... and Projects) **Location** : Devens, MA **Position Summary** The Principal Scientist is a subject matter expert and process/project owner for biologic drug… more
- Merck (Rahway, NJ)
- …barriers to reimbursement and market access, and provide input into clinical , regulatory, payer/access, marketing and evidence generation strategies and programs. + ... (AMCP) dossiers for US payers, and Global Value Dossiers. + Develop supplementary clinical data package in close partnership with markets and HTA statistics group… more
- Merck (West Point, PA)
- …in and/or leads cross-divisional technical teams focusing on late-stage clinical process development, characterization, and/or technology transfer and validation ... Biological Engineering, Biomedical Engineering, Bioprocessing, Business, Chemical Engineering, Chromatography, Clinical Process, Column Chromatography, Communication, Data Analysis, Data Interpretations,… more
- Charles River Laboratories (Mattawan, MI)
- …and education are added correctly. **Job Summary** We are seeking an **Senior Associate Scientist ** for our **Bioanalytical Team** site located in **Mattawan, ... MI** . The following are responsibilities related to the **Senior Associate Scientist ** : An Senior Associate Scientist in Laboratory Sciences is… more
- Cedars-Sinai (Los Angeles, CA)
- …will empower tomorrow's medicine? **Dr. Piotr Slomka, Ph.D. is looking for a Research Associate Data Scientist to join a diverse team!** The Slomka Laboratory ... emission tomography (PET)/computed tomography (CT) angiography imaging. The Research Associate Data Scientist participates in biomedical research projects… more
- Charles River Laboratories (Cleveland, OH)
- …career that you can feel passionate about. **Job Summary** We are seeking a Senior Associate Scientist for our Manual Ion Channel Testing team at our Safety ... Ensure scientific integrity of studies with minimal oversight + Function as a Principal Investigator, Individual Scientist and/or Study Director as assigned with… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …who can contribute to the excellence of our academic community. **Description** The Associate Academic Research Scientist performs a wide range of highly ... + With the approval of the responsible faculty director, may be principal investigators on funded proposals. + Performs other responsibilities as required. OTHER… more
- Actalent (Carlsbad, CA)
- …Manufacturing, and Controls (CMC) and other relevant disciplines such as Clinical and Toxicology. The position also includes authoring scientific reports and ... or MS with at least 5 years (Sr. Research Associate ) or 10 years (Assistant Director) of industry experience...discipline. + Ph.D. with at least 2 years (Sr. Scientist ) or 7 years (Assistant Director) of industry experience… more
