- Genmab (NJ)
- …compassionate, candid, and purposeful, and our business is innovative and rooted in science . We believe that being proudly authentic and determined to be our best ... feel like a fit? Then we would love to have you join us!Role:The Associate Director acts as a statistical expert supporting the clinical development of compounds as… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …supporting company initiatives. Qualifications:Education and Experience: Bachelor's Degree in Life Science required.M.S./PhD. preferred in a scientific ... diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and… more
- Merck & Co. (North Wales, PA)
- …strategic initiative teams Education and Minimum Requirement :BA/BS in Computer Science , Statistics, Applied Mathematics, Life Sciences , Engineering ... 9 years SAS programming experience in a clinical trial environment.MS in Computer Science , Statistics, Applied Mathematics, Life Sciences , Engineering or… more
- Genmab (NJ)
- …like a fit? Then we would love to have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for ... compassionate, candid, and purposeful, and our business is innovative and rooted in science . We believe that being proudly authentic and determined to be our best… more
- Merck & Co. (San Francisco, CA)
- …development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an experienced ... therapeutic areas and modalities to drive portfolio impact from discovery through life -cycle management. The team is externally visible and continues to be at… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJoin Our Team as an Associate Principal Scientist/ Associate Director in Biologics Drug Substance Commercialization!Are you ready to make a ... cross-functional teams to foster collaboration and innovation.Document Excellence: Author regulatory and technical documentation, ensuring all processes align with… more
- Aequor (North Creek, WA)
- …AI, automation, or other technical areas a plus Education: BS degree in life sciences , biotechnology, or engineering, biochemistry, or related discipline Hard ... Summary: We are seeking an experienced, highly motivated Research Associate to join our Manufacturing Science and...Adherence to laboratory safety guidelines and, SOPs, and other regulatory requirements Must be willing and able to work… more
- Merck & Co. (North Wales, PA)
- …clinical drug development, project management, and/or medical field experienceDegree in life sciences , preferred.Experience in planning and executing clinical ... engagements. This includes the ability to:--Strong knowledge of clinical research regulatory requirements (eg, GCP and ICH) Proven ability to manage competing… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …a marketing role within the pharmaceutical industry Experience in pharmaceutical industry/ life science brand marketing strategy and planning; experience within ... you in? Are you ready to experiment with us? The Position The Associate Director Consumer Marketing will be responsible for supporting the development and execution… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …interact with all levels within the organization.RequirementsBachelor's degree in Engineering, Life Sciences , or related field (required).Advanced degree (MS, ... global biotechnology company dedicated to treating, and one day curing, life -threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced… more
- Abbott (Alameda, CA)
- …work for diversity, working mothers, female executives, and scientists. The Opportunity This Associate Director Regulatory Affairs - APAC will work on-site at ... helps people live more fully at all stages of life . Our portfolio of life -changing technologies spans...Diabetes Division. As a manager, the function of an Associate Director Regulatory Affairs, APAC (Asia Pacific)… more
- Organon (Plymouth Meeting, PA)
- …( Associate Director) is responsible for developing and implementing Regulatory Chemistry, Manufacturing & Controls (CMC) strategies for assigned small molecule ... CMC dossiers for programs in clinical development, marketing applications and post-approval life cycle maintenance phases. The Associate Principal Scientist may… more
- Katalyst HealthCares and Life Sciences (Columbia, MD)
- …Maintains awareness of and utilizes current best practices for use of regulatory business systems within the group. Responsible for filing necessary applications and ... facilitate project team meetings. Familiarity with US and other international regulatory requirements for dossiers Superior oral and written communication skills… more
- Bristol-Myers Squibb Company (Princeton, NJ)
- …activities for the pipeline and supports late stage portfolio for regulatory , translational development and life cycle management. Translational Development ... Working with Us Challenging. Meaningful. Life -changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything… more
- IQVIA, Inc. (Durham, NC)
- …of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections ... issues as appropriate. *Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF)… more
- Charles River (Charleston, SC)
- …the health and well-being of people across the globe. Whether your background is in life sciences , finance, IT, sales or another area, your skills will play an ... quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies.… more
- Tiger Analytics (Jersey City, NJ)
- …hands-on experience in demand forecasting and resource allocation within the pharmaceutical and life sciences sector . The ideal candidate will also possess ... models that can adapt to changes in market dynamics, regulatory shifts, or product life cycle stages....7 years in data analytics and forecasting in the pharma/ life sciences domain Strong expertise in time-series… more
- Charles River (Rockville, MD)
- …the health and well-being of people across the globe. Whether your background is in life sciences , finance, IT, sales or another area, your skills will play an ... is as follows: Sun-Wed 12:00pm - 10:30pm The QC Associate I is responsible for performing in-process, release and...With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address… more
- dsm-firmenich (Belvidere, NJ)
- Associate Operator - Production Location: Belvidere, NJ (US) Onsite 12 - Hour Rotating Shifts As an Associate Operator , you will be responsible for producing ... Current Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs), safety/ regulatory requirements, and Site goals. This position is overtime… more
- Mount Sinai Hospital (New York, NY)
- …regulatory authorities. Performs other duties as required. Qualifications Bachelors Degree in life sciences or BSN. 1-2 years experience in relevant Clinical ... Job Description The Clinical Research Associate I monitors all aspects of clinical research...monitors all aspects of clinical research trial(s) Clinical study life -cycle responsibilities including site management, ongoing maintenance and closure… more
