- Insmed Incorporated (Bridgewater, NJ)
- …settingExpert knowledge of relevant guidance including, but not limited to International Committee of Medical Journal Editors (ICMJE), Pharmaceutical Research ... Millennials™ lists.OverviewThe Director, Scientific Publications is a core member of Medical Strategy and Communications team and leads the development and execution… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …including KOLs and Principal Investigators. Essential Functions Support the VP Medical /Scientific Development as the US/ international clinical lead for DCR-PHXC ... trials Ensure compliance with SOPs, ICH, GCP and other national and international regulatory requirements Work with the VP Medical /Scientific Development,… more
- Tris Pharma (Monmouth Junction, NJ)
- …addressing unmet patient needs. We have more than 150 US and International patents (including applications) and have marketed several branded and generic products ... US, have licensed our products in the US and international markets, and have a robust pipeline of innovative...Pain therapeutic area to serve as Senior or Executive Medical Director. Title and salary commensurate with experience. The… more
- Catalent (St. Petersburg, FL)
- …4 GMPs, 21 CFR Parts 111/210/211 (FDA), ISO, and related International Regulations affecting pharmaceutical products and medical devices ... / investigations affecting Catalent sites 50-60% travel expectations (domestic & international ) Other duties as assigned The Candidate: High School diploma, required… more
- Catalent (St. Petersburg, FL)
- …Volume 4 GMPs, 21 CFR Parts 111/210/211 (FDA), ISO, and related International Regulations affecting pharmaceutical products and medical devices Working knowledge ... identified, mitigated, and communicated 40% travel expectations annually (domestic & international ) Other duties as assigned The Candidate: Bachelor's Degree ,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... rare diseases and immune disorders.Summary The Associate Director, Global Oncology Medical Affairs, Medical Intelligence is responsible for leading conference… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Medical Writing & Disclosure Department of the GCTO ( Global Clinical Trial Operations) organization prepares a variety of regulated documentation ... and data sharing with external researchers. - The Specialist (Disclosure Medical Writer) will be primarily responsible for preparing clinical study registration… more
- Lundbeck (Boston, MA)
- …Connecticut, and Rhode IslandPOSITION SUMMARY:The MSL, Psychiatry will apply medical and scientific experience, subject matter knowledge, and skills in ... supporting medical strategies for Lundbeck compounds. Maximizes and leverages key...teaching TRAVEL: Willingness/Ability to travel up to 50-75% domestically. International travel may be required. This position will be… more
- Merck & Co. (North Wales, PA)
- Job Description Description: The Associate Principal Scientist, Oncology Publications Medical Writing, works with scientists in our company's Research Labs and ... and Real-World Evidence, Global Discovery, Preclinical and Translational Medicine, Global Medical and Scientific Affairs, and Global Regulatory Affairs and Clinical… more
- Taiho Oncology (New York, NY)
- Sr. Medical Science Liaison New Jersey, USA New York, NY, USA Philadelphia, PA, USA Req #372 Monday, May 20, 2024 Looking for a chance to make a meaningful ... Value Proposition: Exciting opportunity to join a team of Medical Science Liaisons and collaborate with a dynamic and...required to set up a home-based office. Domestic and international travel may include spending time at cancer trial… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... to the CSPV and key business function and collaborate with RD and Medical Affairs Quality to provide clinical safety QA advise wherever necessary. Ensure… more
- Tris Pharma (Monmouth Junction, NJ)
- …addressing unmet patient needs. We have more than 150 US and International patents (including applications) and have marketed several branded and generic products ... US, have licensed our products in the US and international markets, and have a robust pipeline of innovative...FUNCTIONS Responsible for generation of key study documents and medical oversight of clinical study conduct; Collaborates closely with… more
- Tris Pharma (Atlanta, GA)
- …medicines addressing unmet patient needs. We have over 150 US and International patents - including applications - and several marketed branded and generic ... products in the US We have licensed our products in the US and international markets and have a robust pipeline of innovative products spanning neuroscience and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... and global reorganization. This role will work closely with regional and international Daiichi Sankyo colleagues, as well as, with external entities to ensure… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... be a key and visible expert leader, he/she will engage the clinical, Medical Affairs and commercial organization and drive the product evidence strategies to ensure… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. A key focus will be… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines.Responsibilities:Lead and implement the… more
- Eisai, Inc (Raleigh, NC)
- At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care ... engineering and operations support type roles. Broad knowledge of relevant FDA, International Council for Harmonization (ICH), and EU guidelines coupled with the… more
- Catalent (Philadelphia, PA)
- …degree is preferred Minimum of 5 years in a Pharmaceutical or Medical industry is required Previous Supervisory experience is preferred Good computer skills, ... initiatives Generous 401K match and Paid Time Off accrual Medical , dental and vision benefits effective day one of...around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... to work independently as well as collaboratively in an international matrixed team environment.Strong communication and presentation skills. Strong interpersonal… more
