1116 associate director jobs found

Associate Director Inpatient Medical Services (RN) St. Joseph's Addiction Treatment and Recovery Centers Location: Inpatient Facility - Medical - Saranac Lake, NY Shift/Schedule: Monday-Friday, 8:00am-4:30pm Pay Range: $77,931.00/year to $95,465.48/year Position Type/Expected Hours of Work: Full Time/40+ hours per week. (Hours and schedules may vary depending on company need and workload. Employees will be given as much advance notice as possible when such changes occur. Position Summary: Under the direction of the Inpatient Services Director, the Associate Director of Inpatient Medical Services is responsible for medical services to residents and supervising all medical staff. Qualifications and Requirements: NYS Registered Nurse Knowledge of modern principles and practices of alcohol and chemical dependency programs, knowledge of current NYS DOH nursing and medical operations regulations and medical supervisory experience. Essential Duties: Supervising daily...

New York Institute of Technology seeks an Associate Director of Pipeline Programs at its Jonesboro, Arkansas campus to build a strong pre-med pipeline for NYITCOM. The role focuses on outreach to K-12 and postsecondary partners, coordinating Peer Outreach Mentors, and coordinating with admissions for pathway initiatives. The position requires a Bachelor's degree and experience in program development, with travel and evening/weekend work as needed. #J-18808-Ljbffr

The Associate Director, Medical Publications (CNS) is responsible for supporting the implementation and execution of the global medical publication strategy and deliverables for the CNS therapeutic area. This role ensures the timely, accurate, and compliant communication of scientific and clinical data through congress abstracts, posters, manuscripts, and other peer-reviewed outputs. Working within the CNS Medical Communications team, the Associate Director partners with cross-functional stakeholders including Clinical Development, Global Integrated Evidence & Innovation (GIE&I), Medical Strategy, Core Content, and external vendors to execute high-quality publication activities aligned with overall medical strategy. The Associate Director reports to the Director, Medical Publications (CNS) and plays a key role in driving operational excellence in publication execution while contributing to strategic planning and ensuring adherence to scientific and regulatory standards....

Associate Director, Medical Science Liaison, Cardiac Electrophysiology Johnson and Johnson is currently seeking an Associate Director, Medical Science Liaison, Cardiac Electrophysiology for the Frontier Region. Candidate should be based around Frontier area. Major Duties & Responsibilities: Support the development and implementation of strategic engagement plans to establish and maintain relationships with KOLs, surgeons, operating room staff, and relevant medical societies in the cardiac ablation field. Act as a scientific authority in cardiac electrophysiology, providing medical and scientific education to internal and external stakeholders. Collaborate with cross-functional teams, including Product Management, Clinical Affairs, Marketing, Scientific Affairs, and Research & Development, to provide scientific input and insights. Communicate & streamline complex scientific information effectively to healthcare professionals, ensuring a clear understanding...

A pharmaceutical company based in Honolulu is seeking an Associate Director, Scientific Communications to manage the execution of core scientific communications strategies. This role will oversee the creation of content assets and manage the global publications plan, ensuring scientific accuracy and compliance. Ideal candidates should hold an advanced scientific degree and have over 7 years of experience in Medical Affairs, with strong project management and collaboration skills. A competitive salary range is offered, with various company benefits. #J-18808-Ljbffr

Job Level : Associate Director, Medical Review (MLR) Location : Home-based in USA Job Overview: IQVIA Pharma Review provides outsourced medical copy review and approval services and advisory services to the pharmaceutical industry. As a Final Medical Content Approver, you will act as the primary medical and scientific point of contact providing final approval and expert advice to our clients in line with the requirements of the FDA (FDCA) / PhRMA / FTC for pharmaceuticals and medical devices on assets for clients. You will be expected to be part of the relevant content review teams eg Project/ Product Review Teams (PRT). In this role and as part of the Medical Quality and Compliance team you will be working alongside and as part of the IQVIA Pharma Review Account Teams to deliver a seamless and consistent approach to content approval and consultative compliance advice to the US based clients and business and provide some account management services. In...

Job Title: Associate Director of Medical Operations (ADMO) Location: Multi-site (Regional) Reports To: Director of Medical Operations Position Summary: The Associate Director of Medical Operations (ADMO) is a strategic and medical leadership role responsible for the medical quality, performance, development, and engagement of the DVM teams across a portfolio of hospitals. The ADMO will report to the Director of Medical Operations and will act as the direct link from Ethos medical leadership to the local medical teams. The ADMO partners with the Sr. Division Leader, Operational Support Manager, Hospital Directors, and local Medical Directors to drive financial success through operational efficiencies and high-quality medicine. The ADMO supports Medical Directors in the region to ensure delivery of high-quality, evidence-based medicine while aligning medical initiatives with organizational goals. The ADMO serves as a coach, mentor, and resource for hospital-level MDs and is...

The Associate Director, Medical Publications (CNS) is responsible for supporting the implementation and execution of the global medical publication strategy and deliverables for the CNS therapeutic area. This role ensures the timely, accurate, and compliant communication of scientific and clinical data through congress abstracts, posters, manuscripts, and other peer-reviewed outputs. Working within the CNS Medical Communications team, the Associate Director partners with cross-functional stakeholders including Clinical Development, Global Integrated Evidence & Innovation (GIE&I), Medical Strategy, Core Content, and external vendors to execute high-quality publication activities aligned with overall medical strategy. The Associate Director reports to the Director, Medical Publications (CNS) and plays a key role in driving operational excellence in publication execution while contributing to strategic planning and ensuring adherence to scientific and regulatory standards....

This is what you will do: The Associate Director Strategic Planning & Execution, US Medical Affairsis responsible forthe execution of strategic initiatives within the US Medical Affairs organization and will partner with TA Leadership teams and cross functionally to execute on projects in line with the functions overall strategic goals. This position will analyze, resolve, andcommunicate onkey strategic programsallowing forUS Medical Affairs Leadership to make informed decisions that will contribute to the overall success of the function. This position will apply good project management techniques toinsure inscope,on-time, on budget results. You willbe responsible for: Strategic Partnership: Develop annual enterprise strategy for assigned TA and/or Function and ensure effective, efficient, andequitabledelivery of key strategic programs and operational activities Oversight of business progress against performance targets through outcomes and metrics tracking/reporting...

Associate Director, Global Medical Affairs Publication Operations We are searching for the best talent for an Associate Director, Global Medical Affairs Publication Operations located in Raritan, NJ. The Associate Director, Global Medical Affairs Publication Operations will provide expert reviewing, writing, and editing support to ensure timely production of high-quality documents (abstracts, posters, slide presentations, manuscripts, letters to editor, etc.) for publication in medical/scientific journals or presentation at medical/scientific meetings, and maintain compliance with all company policies/procedures and applicable industry standards/guidelines. You will be responsible for : Responsible for scientific publication writing including abstracts, posters/oral presentations, and manuscripts, etc., and responsible for the overall production of publications and compliance with standard operating procedures/industry standards. Familiar with the overall publication...

The Associate Director, Medical Publications (CNS) is responsible for supporting the implementation and execution of the global medical publication strategy and deliverables for the CNS therapeutic area. This role ensures the timely, accurate, and compliant communication of scientific and clinical data through congress abstracts, posters, manuscripts, and other peer-reviewed outputs. Working within the CNS Medical Communications team, the Associate Director partners with cross-functional stakeholders including Clinical Development, Global Integrated Evidence & Innovation (GIE&I), Medical Strategy, Core Content, and external vendors to execute high-quality publication activities aligned with overall medical strategy. The Associate Director reports to the Director, Medical Publications (CNS) and plays a key role in driving operational excellence in publication execution while contributing to strategic planning and ensuring adherence to scientific and regulatory standards....

Associate Director / Director, Medical Information Cambridge, Massachusetts, United States Cognito Therapeutics Associate Director / Director, Medical Information Reports to: Head of Medical Affairs About the Role Cognito Therapeutics is seeking a driven, scientifically rigorous Associate Director/Director of Medical Information to build and lead the Medical Information (MI) function from the ground up. This is a hands-on role suited to a motivated individual contributor who wants to establish strong operational foundations and deliver high-quality scientific content in the Alzheimer's and neurocognitive disease space. The role will design and implement core MI capabilities — inquiry management systems, standard response documents, and medical review workflows — positioning Cognito for its first commercial launch and for scaling as the pipeline grows. The role will also contribute to Cognito's Medical Affairs AI initiatives, bringing scientific and operational judgment to the...

Company Description EVERSANA INTOUCH® is a global, full-service marketing agency network serving the life sciences industry, and is the first – and only – agency network to be part of a fully integrated commercialization platform through EVERSANA®. We provide next-generation creative and media services, enterprise solutions and data analytics services for clients. We get fired up when people talk about getting—and staying—healthy. That’s where we find our inspiration: in the very human experiences of patients, doctors, and even each other. Then, we collaborate on ways to make caring for one’s health more achievable, connecting patients and physicians with the information and tools they need. We embrace diversity in backgrounds and experiences. Improving patient lives around the world is a priority, and we need people from all backgrounds and swaths of life to help build the future of the healthcare and the life sciences industry. We believe our people make all the difference in...

Associate Director, Medical Affairs Location: Cambridge, MA (100% Remote) Duration: 6 Months+ Possible Extension Pay Range: $100-$120/hr Manager Notes: Hybrid preferred. But remote candidates can also be considered. If Hybrid, expected to visit the office at least twice a week. No specific days, depends upon the requirement. High likelihood of further extensions beyond the given end date. Summary & Purpose of the Position Reporting to the Senior Director, Medical Affairs (Adult Cholestatic Diseases), the Associate Director, Medical Affairs, will support and oversee select medical affairs activities related to biliary atresia. This role will contribute to the U.S. medical strategy for elafibranor and the broader Medical Affairs plan for cholestatic diseases. Responsibilities include medical review of non-promotional and promotional content, information responses (in collaboration with Medical Information), scientific communications including poster presentations and...

We are seeking an Associate Director, Medical Writing to lead the development and execution of high-quality clinical and regulatory documentation. This individual will play a key role in shaping document strategy, managing the end-to-end writing process, and ensuring compliance with global regulatory standards. The ideal candidate brings a combination of strong scientific expertise, project leadership, and the ability to collaborate effectively across internal teams, external partners, and vendors. This role requires both hands‑on writing capabilities and the ability to guide complex, cross‑functional initiatives. Key Responsibilities Clinical & Regulatory Writing Leadership Serve as the lead medical writer across one or more clinical programs Author and oversee the development of key clinical and regulatory documents, including: Clinical study protocols and associated documents (e.g., informed consent forms) Clinical study reports (CSRs) Development Safety Update...

A global biopharmaceutical company is seeking an Associate Director, Scientific Communications, responsible for managing the execution of scientific communication strategies. This role ensures the creation of core content assets while overseeing the global publication plan. Applicants should have an advanced scientific degree and significant experience in Medical Affairs or Scientific Communications. The position offers a competitive salary and comprehensive benefits including medical and dental coverage, 401(k) match, and more. #J-18808-Ljbffr

The Associate Director for Medical Student Financial Aid serves as the primary financial aid administrator and financial wellness leader supporting students enrolled at the Virginia Tech Carilion School of Medicine (VTCSOM). Reporting jointly to the Vice Dean of the Virginia Tech Carilion School of Medicine and the Associate Vice Provost for University Scholarships and Financial Aid, this position provides strategic leadership in the administration of financial aid programs while advancing student financial success through personalized advising, financial wellness education, operational excellence, and collaborative partnerships. The Associate Director serves as the Virginia Tech Carilion School of Medicine's recognized subject matter expert in medical student financial aid, educational financing, physician debt management, loan repayment strategies, and financial wellness. The position provides strategic leadership in the administration of federal, institutional, scholarship, and...

A leading pharmaceutical company is seeking an Associate Director, Scientific Communications to manage global scientific communication strategies for their therapeutic portfolio. This role involves delivering operational results through effective oversight and guidance in the development of scientific content and the publication plan. The ideal candidate will possess an advanced scientific degree and have significant experience in medical affairs, scientific communications, and team leadership. Strong interpersonal skills and a strategic mindset are essential for success in this role. #J-18808-Ljbffr

Job Description Job Description Benefits: 401(k) matching Employee discounts Health insurance Paid time off Parental leave Are you a compassionate leader with a passion for animal welfare? Humane Fort Wayne is seeking an Associate Director of Animal & Medical Care to lead our shelter's medical, behavioral, and animal care programs. In this role, you'll guide a dedicated team while ensuring every animal receives exceptional care, enrichment, and the best opportunity for a positive outcome. What You'll Do Lead Animal Health & Welfare Oversee all aspects of shelter medical care, including intake, treatment, vaccinations, disease prevention, and recovery. Manage medical programs such as surgery coordination, isolation and quarantine, foster medical support, neonatal care, and humane end-of-life services. Monitor medical outcomes and implement improvements that enhance animal health and welfare. Advance Behavior & Enrichment Develop and oversee...

Driven by a bold pursuit of science and fueled by an unwavering commitment to patients, Sun Pharma is a leading global pharmaceutical company, providing high-quality medicines trusted by healthcare professionals and patients. As part of our mission to Reach People and Touch Lives, we deliver Innovative Medicines, Generics and Consumer Healthcare products that improve the lives of millions of people. With a broadly diversified portfolio of products that span multiple therapeutic areas, we improve access to effective, affordable treatments that promote better health and well-being. Reaching People. Touching Lives. Job Summary Sun Pharma is seeking a strategic and dynamic Associate Director, Marketing (DTC & HCP) - Medical Dermatology to serve as a key leader within the U.S. Medical Dermatology Marketing organization. This position reports to the Senior Director, Marketing – Medical Dermatology and the work location is Princeton, NJ (3 days in the office per week). This role...

## Associate Director, Global Medical Affairs, SLEPrinceton - NJ - USFind out how well you match with this job**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 but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more:...

A leading pharmaceutical company in New Jersey seeks an Associate Director, Scientific Communications to manage the execution of a global medical communications strategy. In this role, you will oversee the development of core content assets, ensure regulatory compliance, and provide guidance to a team of medical writers. Ideal candidates will have an advanced scientific degree and extensive experience in pharmaceutical industry communications, with a strong focus on CNS therapeutic areas. Competitive compensation package offered. #J-18808-Ljbffr

Who We Are At Dendreon, we’re transforming the battle against cancer with personalized immunotherapy. Our flagship product, PROVENGE® (sipuleucel‑T), was the first FDA‑approved immunotherapy for metastatic castrate‑resistant prostate cancer, utilizing a patient’s own immune cells to fight the disease. If you’re driven by the opportunity to make a meaningful impact on cancer patients’ lives, we invite you to join our team. With Immunotherapy Manufacturing Facilities in Seal Beach, CA, and Union City, GA, a strong Research & Development group in Seattle, WA, and a highly skilled Commercial team across the nation, Dendreon is at the forefront of cancer treatment innovation. Core Values Put Patients First: Every day is an opportunity to improve the lives of those living with cancer. Act with Integrity: We commit to transparency, honesty, and always doing what’s right. Build Trust: Trust is earned through candid, open communication and a collaborative approach. Raise the Bar:...

Associate Director, Medical Review (MLR) Location: Home-based in USA IQVIA Pharma Review provides outsourced medical copy review and approval services and advisory services to the pharmaceutical industry. As a Final Medical Content Approver, you will act as the primary medical and scientific point of contact providing final approval and expert advice to our clients in line with the requirements of the FDA (FDCA) / PhRMA / FTC for pharmaceuticals and medical devices on assets for clients. You will be expected to be part of the relevant content review teams eg Project/ Product Review Teams (PRT). In this role and as part of the Medical Quality and Compliance team you will be working alongside and as part of the IQVIA Pharma Review Account Teams to deliver a seamless and consistent approach to content approval and consultative compliance advice to the US based clients and business and provide some account management services. In addition, you will be expected to support...