177 associate director jobs found

Job Description Associate Director, Medical Affairs Operations & Patient Advocacy Job Description Terns Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing a portfolio of small-molecule product candidates to address serious diseases, including oncology, obesity, and non-alcoholic steatohepatitis (NASH). Terns' programs are based on mechanisms of action that have achieved proof-of-concept in clinical trials in indications with large unmet needs. Headquartered in Foster City, CA, Terns combines extensive research and development experience in drug development with a capital-efficient drug discovery and clinical development model to advance its growing pipeline of medicines. We have an exciting opportunity within Medical Affairs for an Associate Director, Medical Affairs Operations & Patient Advocacy. Essential Duties and Responsibilities: The candidate will work in partnership with the Director, Medical Affairs and the Leadership Team to manage...

Company DescriptionDeciphera is a biopharmaceutical company focused on discovering, developing and commercializing important new medicines to improve the lives of people with cancer. We are leveraging our proprietary switch-control kinase inhibitor platform and deep expertise in kinase biology to develop a broad portfolio of innovative medicines.In addition to advancing multiple product candidates from our platform in clinical studies, QINLOCK is Deciphera's FDA-approved switch-control kinase inhibitor for the treatment of fourth-line gastrointestinal stromal tumor (GIST). QINLOCK is also approved for fourth-line GIST in Australia, Canada, China, and Hong Kong.Deciphera (NASDAQ: DCPH) is a publicly traded company headquartered in Waltham, Massachusetts. Our state-of-the-art research facility is located in Lawrence, Kansas. We offer an outstanding culture and opportunity for personal and professional growth based on our "PATHS" Core Values:Patients - places the importance of...

Join a Legacy of Innovation 110 Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 15,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. Under the Group's 2025 Vision to become a "Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary The primary responsibilities of this position are to write, with minimal supervision of the lead author (Director, Medical Writing) complex documents including...

Join a Legacy of Innovation 110 Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 15,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. Under the Group's 2025 Vision to become a "Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. S ummary: The Associate Director, Field Medical Training will be responsible for the development, implementation, and continuous improvement of a strategic and...

Job Description Salary: Ventyx Biosciences, Inc. is a clinical-stage, public biopharmaceutical company focused on advancing new therapies for millions of people living with inflammatory diseases and autoimmune disorders. We are developing novel and differentiated therapeutics that target both the innate and adaptive immune system. Our clinical-stage programs include an allosteric TYK2 inhibitor for the treatment of a broad range of autoimmune diseases, an S1P1 receptor modulator for the treatment of ulcerative colitis, and a peripheral inhibitor of the NLRP3 inflammasome, which is a mediator of multiple inflammatory conditions. Join this team of life science professionals to bring this portfolio of programs to fruition. The Opportunity: Associate Director Medical Writing This position will be responsible for leading the medical writing activities for one or more development programs. This role will play a critical part in managing the timely development and completion of clinical...

Lexicon Pharmaceuticals is currently searching for a highly collaborative, knowledgeable and detail oriented Associate Director of Medical Information. We have offices om the Woodlands Texas and Bridgewater; New Jersey. However, this position may be a remote role with occasional travel to our offices and major medical congresses.Job Summary:The Associate Director of Medical Information is a critical member of the Medical Affairs team and will interact extensively with both internal stakeholders to plan, develop, coordinate, and execute our Medical Information strategy and tactics, and be the primary liaison with third-party call center for incoming Medical Information Requests (MIR). These activities include but are not limited to the development and maintenance of the department product knowledge library and assuring accurate and up-to-date annotation of all Medical resources, development of standard and custom responses to medical inquiries, tracking call center and Field Medical...

A medical technology company has an open position for a Telecommute Medical Science Liaisons Associate Director. Must be able to: Provide input into engagement plans with key external stakeholders Contribute to medical affairs business plan Lead and support therapeutic area advisory boards Qualifications for this position include: MD, PhD in neuroscience or similar advanced doctoral degree 5 years documented professional experience Expertise in scientific and clinical data review and interpretation Project leadership and people management skills Superior communication skills Ability to develop, influence and maintain relationships with significant key opinion leaders

As an Associate Director, Field Medical Affairs, you will play a pivotal role as a field-based professional within dermatology. Use your expertise that will provision the business objectives across the product life cycle. We deliver strategic and operational support by establishing, developing, maintaining scientific exchange with medical specialists, health care professionals, and payers, aligned with our strategic objectives. We provide clinical and health economic information that enhances th

Job Description Description Altimmune (NASDAQ: ALT) is a clinical-stage biopharmaceutical company focused on developing treatments for obesity and liver diseases. Our pipeline includes next-generation peptide therapeutics for obesity, NASH (ALT-801), and chronic hepatitis B (HepTcell™). Job Description The Company is seeking an Associate Director/Director, Medical Affairs to be responsible for providing scientific and clinical support Altimmune's medical products/therapeutic area and for the development/implementation of activities with leadership and external experts to drive important projects with Medical Affairs. The candidate will be expected to ensure that all programs meet the quality and safety standards required by the medical community and regulatory agencies. The candidate will report to the Chief Medical Officer. Essential Functions * Leads efforts in recognizing and integrating substantive relationships with leadership and external experts in specific therapeutic...

A staffing and recruiting agency is searching for a person to fill their position for a Remote Medical Associate Director. Core Responsibilities of this position include: Developing, maintaining and executing comprehensive medical education plans for assigned therapeutic areas Serving as OGE lead on cross-functional medical disease teams Executing ongoing evaluation / monitoring of supported educational initiatives Position Requirements Include: Execute ongoing evaluation / monitoring of supported educational initiatives Minimum of 5 to 7 years of experience Understanding of PhRMA, OIG, and ACCME guidelines and policies as well as other regulatory, legal, ethics/compliance guidelines/regulations MS and/or BS required

Job Description Company Description Deciphera is a biopharmaceutical company focused on discovering, developing and commercializing important new medicines to improve the lives of people with cancer. We are leveraging our proprietary switch-control kinase inhibitor platform and deep expertise in kinase biology to develop a broad portfolio of innovative medicines. In addition to advancing multiple product candidates from our platform in clinical studies, QINLOCK® is Deciphera's FDA-approved switch-control kinase inhibitor for the treatment of fourth-line gastrointestinal stromal tumor (GIST). QINLOCK is also approved for fourth-line GIST in Australia, Canada, China, and Hong Kong. Deciphera (NASDAQ: DCPH) is a publicly traded company headquartered in Waltham, Massachusetts. Our state-of-the-art research facility is located in Lawrence, Kansas. We offer an outstanding culture and opportunity for personal and professional growth based on our "PATHS" Core Values: Patients - places the...

Job Description Position Summary: The Associate Director, Global Medical Affairs, Ophthalmology is a key member of the Global Medical Affairs team who will work closely with medical affairs and cross-functional stakeholders to implement key aspects of the Global Medical strategy for ophthalmology and potential global launches of pegcetacoplan in geographic atrophy (GA) secondary to age-related macular degeneration (AMD). These activities may include data generation, insight gathering, and scientific communications/publications, as the medical affairs team supports launch readiness in the ophthalmology space. Key Responsibilities Include: * Implement key aspects of GMA strategy for pegcetacoplan in ophthalmology * Drive and/or assist in development and implementation of evidence generation strategy (Phase IV, real-world evidence/HEOR, post hoc analyses, investigator initiated trials and collaborative research), * Drive and/or assist in insight gathering, scientific communications...

Job Description POINT Biopharma is an innovative, high-performance company focused on a hard problem: creating new cancer therapies that are more effective and have fewer side effects than traditional treatments. Our products are targeted radioligands, a technology that hold significant promise to treat cancer. Our company is growing rapidly: we just announced a phase 3 clinical trial for our novel radioligand based prostate cancer treatment, established our U.S. manufacturing center in Indianapolis, and have a pipeline of next generation oncology products in development. We are a creative and agile team accountable to a high standard: to be uniquely better. If you are searching for new and uniquely better career path, you should consider joining the POINT team. TO BE CONSIDERED, APPLICANTS MUST BE LEGALLY ENTITLED TO WORK IN THE USA. Location of work The position will be working remotely with the anticipation of travel for team and client meetings. To work in synergy, it is...

Job Description Role Summary The Associate Director, Medical Writing, reporting into the Executive Director, Medical Writing and Regulatory Affairs, will work in partnership with cross-functional teams to generate and lead the development of Clinical and Regulatory documents across all LEXEO programs. This role will be responsible for the planning, development, and oversight of study and program level documents with a focus on accuracy, quality, and compliance. This role will assist in oversight of external partners and process development initiatives and will be an integral contributor to the completion of department and corporate objectives. To be successful in this position, candidates will possess a commitment to excellence, a patient- and team-focused mindset, knowledge of ICH and health authority guidance, and demonstrated leadership in operational and strategic aspects of document development. Location Our work culture is a hybrid model with days in the New York City office...

Primary City/State:Glendale, ArizonaDepartment Name: PCU-ST6 E&W-HospWork Shift: NightJob Category:NursingBanner Health believes leadership matters, and we look for people who share our vision making health care easier, so life can be better. Our leaders are at the front of the health care transformation, planning the future of Banner Health.Join our General Medical Progressive Care Unit at Banner Thunderbird Medical Center and become part of our talented team of professionals.  Our state-of-the-art Level 1 Trauma Facility and General Medical PCU specialize in high level care to patients with a multitude of complex disease processes. We are committed to providing our community with excellent patient care and are ranked as one of the top five hospitals in Phoenix, being recognized for eight high-performing specialties, according to U.S. News Best Regional Hospitals report. Clinical expertise, compassionate patient care and research are important parts of Trauma and...

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: Join Takeda as an Associate Director, US Medical Communications - Gastroenterology (GI) where you will be a strategic partner of the US Medical Communications team responsible for supporting the development and execution of the medical communications strategy across the assigned therapeutic portfolio. You will also be involved in the medical communications Scientific Communication Platform (SCP) and Integrated Communication Platform (ICP) development, and content generation, which may include, but is not limited to, publications, scientific slide decks, field medical tools,...

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: Join Takeda as an Associate Director, US Medical Communications - Hematology and Rare Diseases where you will be a strategic partner of the US Medical Communications team responsible for supporting the development and execution of the medical communications strategy across the assigned therapeutic portfolio. You will also be involved in the medical communications Scientific Communication Platform (SCP) and Integrated Communication Platform (ICP) development, and content generation, which may include, but is not limited to, publications, scientific slide decks, field medical...

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: Join Takeda as an Associate Director, US Medical Clinical Research where you will provide clinical research leadership to ensure successful strategic implementation of all US Medical Clinical Research including, Medical Affairs Company Sponsored Studies (MACS) and collaborative studies. As part of the US Medical team, you will report to the Head, US Medical Clinical Research. This is a hybrid role based in Lexington, MA. How you will contribute: •    Partner with Head of US Medical and Director of Clinical Research to translate strategy into efficiently executable research plan;...

For Current Gilead Employees and Contractors: Please log onto your Internal Career Site to apply for this job. Job Description Gilead Sciences is a research-based biopharmaceutical company that discovers, develops, and commercializes innovative medicines in areas of unmet medical need including virology, oncology, and inflammation. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gilead has established employee resource groups to support diversity and inclusion , and provides a competitive benefit package including flexible work options and exceptional support for the family and the individual. www.gilead.com Medical Writing is a global, dynamic, and diverse team of highly skilled professionals. We work collaboratively to advance the strategy and create...