- Astellas Pharma (Northbrook, IL)
- …and accountability for clinical pharmacology from first-in human through approval , including post -marketing activities for assigned projects. The Director ... Candidates interested in remote work are encouraged to apply. **Purpose and Scope:** The Director , Global Clinical Pharmacology will have ultimate responsibility… more
- Mental Health Association of SCK (Wichita, KS)
- POSITION TITLE : Clinical Director of Outpatient and Addiction Services FLSA CLASSIFICATION: Exempt REPORTS TO: COO POSITIONS SUPERVISED: Staff Therapists and ... Substance Counselors POSITION OVERVIEW: The Clinical Director will be responsible for the...a minimum of two years' experience providing therapeutic services post license. Must be eligible for approval … more
- AbbVie (North Chicago, IL)
- …first in human through approval , including life cycle management and post approval commitments/requirements. You will be expected to communicate/present and ... @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description As a Director within the Clinical Pharmacology Neuroscience Group at AbbVie, you… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …as other research areas centered around rare diseases and immune disorders. **Summary** The Director , Clinical Safety, will be a product safety lead or part of ... management, and provide safety leadership including but not limited to clinical studies, post -marketing surveillance, signal detection and management, important… more
- Boehringer Ingelheim (Ridgefield, CT)
- …benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Director , Clinical Development Strategy Team Member is responsible for ... BI market approach and informs medical affairs efforts where applicable. The Director , Clinical Development Strategy Team Member collaborates cross functionally… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …relating to the preparation / approval of protocols and the conduct of clinical studies to support LCM, post marketing requirements and regional or local ... best of my knowledge. **Job Description** **Job Description for Senior Medical Director , Clinical Science, Marketed Products Development** As the Senior Medical… more
- Boehringer Ingelheim (Ridgefield, CT)
- …which may include engaging with marketplace stakeholders prior to product approval . Demonstrates expert knowledge of TA disease state, treatment guidelines, product, ... adverse event management and the marketplace. The Senior Associate Director works closely with a variety of internal stakeholders,...internal and external stakeholders, in the pre, per and post - launch phase of the product life cycle to… more
- Lilly (Indianapolis, IN)
- …certified in appropriate specialty/subspecialty or have completed the comparable level of post -medical school clinical training relevant to the country of ... to make life better for people around the world. ** Clinical Design Physician - Clinical Design** **Purpose:**...understand the impact of design on speed to protocol approval and study startup. Identify and participate in opportunities… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …JOB DESCRIPTION: + Supports the day-to-day activities of a team of Post -Award Specialists. Monitors workload distribution and raises any concerns to the Research ... Administration Services (RAS) director . + Provides guidance to team members, as appropriate....inter-team meetings to facilitate collaboration between the pre-award and post -award teams, as necessary and appropriate. + Manages … more
- Pfizer (Pearl River, NY)
- …direct experience with all the steps in designing and delivering results of clinical trials by applying extensive expertise and in-depth knowledge of clinical ... research programs and registration activities across one or more clinical projects. The clinician medical monitor ensures successful global program implementation… more
- Pfizer (Pearl River, NY)
- …monitor is accountable for providing medical and scientific expertise and oversight for Clinical Trials and serves as a single point of accountability for design, ... execution, monitoring, delivery and reporting of one or more clinical studies and to ensure patient safety. + The...development strategy for multiple protocols designed to obtain worldwide approval for a compound or group of compounds. +… more
- Taiho Oncology (Pleasanton, CA)
- …projects; provides strategic regulatory guidance especially for CMC during drug development, approval and post approval processes and commercialization, in ... Director , Regulatory Affairs CMC Pleasanton, CA, USA Req...Provides strategic regulatory guidance, especially CMC during drug development, approval and post approval in… more
- Baystate Health (Springfield, MA)
- …institute setting is required. Reporting to the Chief Research Officer, the Director , Sponsored Programs Administration (SPA) a team at the primary Baystate Medical ... to provides administrative, financial, regulatory, and compliance support of Pre-award, Post -award, and Accounting of approximately $20M in research expenditures of… more
- BeiGene (San Mateo, CA)
- …and leads recommendations for RMP/REMS update + Leads the development of safety Post Approval Commitments (PAC) proposals, facilitates the design of PAC proposed ... **General Description:** The Senior Medical Director serves as the Product Safety Physician for...causation + Accountable for output/summary report for inclusion into clinical , filing, and post -market reports + Accountable… more
- Lilly (Indianapolis, IN)
- …leadership, ability to influence, both within and outside the team. The Sr. Director -Medical supports the clinical staff within his/her product or therapeutic ... ensure high quality, timely submissions, and successful commercialization. The Sr. Director -Medical may be delegated such responsibilities as approval authority… more
- Intermountain Health (Murray, UT)
- …Medical Director Hyperbaric Medicine will provide oversight for clinical program development for Hyperbaric services, budgeting, policy and regulatory ... is .85 FTE Clinical and .15 FTE Leadership. As the Medical Director , this position: + Will provide medical direction for all Hyperbaric services associated with… more
- State of Georgia (Fulton County, GA)
- …to the national board exams. 9. Assist Faculty in evaluation of student clinical competencies and experiences. 10. Assist Program Director with assurances of ... Medical Director - Paramedicine (Part-Time) Georgia - Fulton -...Hot (https://careers.georgia.gov/landingpages/education-opportunities-at-team-georgia-11) Education Atlanta Technical College Apr 12, 2024 Post Date Apply for Job Share this Job Sign… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …leads, develops, and implements strategic and tactical support for commercial, post approval regulatory activities for successful and compliant promotion ... Regulatory Affairs, is responsible for the development and execution of the post - approval regulatory strategy, post -marketing commitments, post -marketing… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …disease in the US. This includes supporting and leading projects related to pre- approval and post - approval medical activities in Parkinson's disease (ND0612) ... (edaravone) oral suspension in 2022. The company handles research, clinical development, sales, marketing, medical affairs, and business development functions.… more
- Amicus Therapeutics (Marlow, OK)
- …work collaboratively with Global Medical Operations and Country Medical teams to deliver post approval data generation (IIPs and Phase IV and non-interventional ... Senior Director , Regional Medical Lead, International, Pompe Location Marlow,...Global Medical Operations and Country Medical Teams to deliver post approval data generation activities including investigator-initiated… more