- Pfizer (Groton, CT)
- …VP will report to the Head of Oncology Medical, Pfizer Oncology. + The incumbent will lead the Global Medical Strategy Heads and the Global Medical Strategy ... a senior and respected subject matter expert in the clinical Oncology community, the incumbent will drive Pfizer's presence...the Medical Affairs local teams to unlock the full global potential of our existing and future commercially available… more
- Boehringer Ingelheim (Ridgefield, CT)
- …industry in the healthcare environment + Proven track record on overseeing and running global clinical trial programs managing complex projects and working ... **Description** The Clinical Development Operations Lead (CDOL) is...Experience specific to Obesity/NASH is highly preferred **Senior CDOL ( Director )** + PhD or MD . Specialist with… more
- Boehringer Ingelheim (Ridgefield, CT)
- …the US TA, RWE, FBM, Strategic Engagement, and the global TA teams to lead and implement excellence in clinical development as well as the generation of a ... reflect Boehringer Ingelheim's high regard for our employees. The Director , Clinical Development Strategy Team Member is...guidance and coordinate with the global Evidence Lead to contribute to the clinical trial… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and global regulatory and ethical standards. **Requirements** **Requirements for Director Level:** + MD and retinal specialist from an accredited ... Excellence goals. The optimal candidate will be experienced in clinical research and would be an MD ,...clearly. + Proven track record on overseeing and running global clinical trial programs and working collaboratively… more
- J&J Family of Companies (Hartford, CT)
- …be a member of the Global Medical Affairs team, leading the conduct of a global clinical study using the portfolio of compounds at Janssen with the aim of ... Medical Director , Bladder - Global Medical Affairs...will act as a liaison between the company and clinical investigators. Importantly, they will lead the… more
- Pfizer (New Haven, CT)
- …the role responsibilities. Include any external interactions as appropriate. + Reports to Sr. Director Global Head of PCRU Clinical Operations. + Networks ... Clinical Development and Operations, and participates on/contributes to global clinical research committees (eg CPSDC). **Training** + Participates… more
- J&J Family of Companies (Hartford, CT)
- Senior Clinical Data Analyst - 2406185694W **Description** At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us ... https://www.jnj.com/. Biosense Webster, Inc is recruiting for a Senior Clinical Data Analyst, to be based at anywhere is...anywhere is united states. Biosense Webster, Inc. is the global leader in the science of diagnosing and treating… more
- Pfizer (Groton, CT)
- …regulatory expertise as Global regulatory representative to Product Team(s). As a Director , Lead and coordinate a virtual global regulatory strategy team ... Degree(BA/BS)and 10+ years of experience. MS, PharmD, PhD or MD preferred. Equivalent workplace experience can be considered. +...+ Extensive direct regulatory experience, preferably including as a Global Regulatory Lead and leading a GRST.… more
- Pfizer (Groton, CT)
- …of different regulatory requirements of different sites and countries. + Ability to lead cross-line global initiatives or root cause analysis for quality related ... maintaining 'quality' line-of-sight for assets/protocols within the Pfizer Oncology clinical portfolio. + With this focus, the Asset Quality... portfolio. + With this focus, the Asset Quality Lead (AQL) role brings deep knowledge of Level One… more
- Pfizer (Groton, CT)
- …QUALIFICATIONS:** + Experience with Program Management best practices. + Ability to lead cross-line global initiatives or root cause analysis for quality ... **ROLE SUMMARY:** + Lead as a player/coach the group of Oncology...and Excel skills/experience. **ORGANIZATIONAL RELATIONSHIPS:** + **Within** **Oncology CD&O:** Global Study and Site Operations GSSO, Oncology Clinical… more
- Pfizer (Groton, CT)
- …of different regulatory requirements of different sites and countries. + Ability to lead cross-line global initiatives or root cause analysis for quality related ... **ROLE SUMMARY:** + Lead as a player/coach the group of Asset...+ Responsible for ensuring Level 1 GCP quality for clinical development programs within Pfizer Oncology R&D by establishing… more
- Boehringer Ingelheim (Ridgefield, CT)
- …advisory committees, global regulatory authority meetings, Advisory Boards, Board of Managing Directors, congresses. + Lead strategic projects within GPV (eg ... the opportunity for significant professional development. The (Senior Associate) Director is a key member of global ,...as required to ensure safe use in patients. The Director may also lead a team of… more
- Merck (Hartford, CT)
- …enrollment and retention efforts to achieve study milestones. + Upon Request from Global Clinical Trial Operations (GCTO) + Recommends study sites and identifies ... Director (Medical Science Liaison) is a credentialed (ie, PhD, PharmD, DNP, MD ) Director Level Medical Affairs position and therapeutic and disease expert… more
- Bristol Myers Squibb (Stamford, CT)
- …The Regional Associate Director (RAD) role is field-based and focused on managing a team of Medical Science Liaisons (MSLs). The RAD is responsible for oversight ... of MSLs in support of BMS medicines and all phases of associated clinical trials. The RAD oversees their regional team to ensure disease and product related medical… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Profound experience in patient safety at a pharmaceutical company on a global /corporate level, including clinical development and post-marketing safety + ... TA CRM Team is looking for an experienced Executive Director of Patient Safety Physician with expertise in cardiovascular,...You'll work on a variety of products, both in clinical development and post-marketing drug safety. Ready to make… more
- GE HealthCare (CT)
- …provide medical support to external projects, such as advisory boards, educational activities, clinical study support, etc. As the MSL, you will be responsible for ... cultivating relationships while conveying clinical outcomes about neurology radiopharmaceutical agents via evidence based...based activities. Our Pharmaceutical Diagnostics (PDx) business is a global leader in imaging agents, used to improve and… more
- Boehringer Ingelheim (Ridgefield, CT)
- …This individual will work closely with the Medical Affairs Strategy teams and Global Medical Information (MI) to ensure the timely development of scientific content ... external utilization based on customer needs and aligned with global MI content. This individual is also responsible for...as to help with on-boarding, training and guidance of Clinical Development and Medical Affairs (CDMA) TA team members.… more
- Boehringer Ingelheim (Ridgefield, CT)
- …preferred. + In lieu of a doctoral level research degree, a doctoral level professional clinical degree ( MD , DO, PharmD, etc) AND a Master's degree OR other ... of our benefits please click here. (https://www.boehringer-ingelheim.com/us/careers/benefits-rewards) **Description** Lead the development, implementation, and communication of HEOR strategies… more
- Arvinas (New Haven, CT)
- Arvinas is a clinical -stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases through the ... validated and "undruggable" targets, the company has three investigational clinical -stage programs currently enrolling: vepdegestrant for the treatment of patients… more
- Arvinas (New Haven, CT)
- …. For more information, please visit www.arvinas.com . **Position Summary** The Director , Omnichannel Scientific Communications will lead the strategic planning, ... Arvinas is a clinical -stage biotechnology company dedicated to improving the lives...Arvinas entered into a transaction with Novartis, including a global license agreement for the development and commercialization of… more