12 associate director of development jobs found

Merck Job Description The Developmental and Reproductive Toxicology (DART) group within Nonclinical Drug Safety (NDS), is seeking a highly motivated person with strong technical skills and diligence to conduct in vivo studies as part of a collaborative team supporting drug development programs. The successful candidate will perform in vivo administration of compound, data collection, cesarean sections with fetal examination, and necropsies under limited supervision. The position requires the ability to maintain neat, concise, and accurate records, along with good oral communication skills. The successful candidate will also train and work cross-functionally, assisting other areas within NDS. This position is for a 5-day work week, including coverage of weekends and Holidays on a rotational basis. Specific responsibilities include but are not limited to: Perform assigned tasks that include dose administration by various routes; recording of body weights, food...

Merck Job Description The Executive Director of Materials and Biophysical Characterization plays a critical role in advancing our company's mission. This leader is responsible for providing strategic and technical leadership for materials characterization methodologies, phase screening platforms, and biophysical characterization to enable deep understanding of drug substances and drug products and successful advancement of small molecules, biologics, and vaccines from discovery through development and commercial launch. Reporting to the Associate Vice President of Analytical Enabling Capabilities, the Executive Director will lead a multidisciplinary team of 50-60 talented people managers, scientists, and technical experts across our Rahway, NJ and West Point, PA sites. In this role, you will partner closely with leaders across Discovery, Preclinical Development, Manufacturing, Quality, and Regulatory to ensure our science delivers with excellence across the development...

Alkermes, Inc. The Associate Director position within Clinical Supply Chain provides strategic leadership and oversight for end-to-end supply chain management across multiple clinical programs as part of a growing, dynamic Pharmaceutical Development organization. Serving as the primary point of contact, the Associate Director collaborates closely with Clinical Operations, Regulatory Affairs, Quality, Internal & External Manufacturing, and other Clinical Supply Chain personnel, leading complex supply activities that often require multinational coordination. Additionally, this role is responsible for building and maintaining strong partnerships with both internal and external stakeholders, ensuring alignment with organizational objectives. The successful candidate will demonstrate leadership in a highly collaborative team environment, driving the successful development and delivery of new drugs. Responsibilities Oversee, update, and monitor program budgets while ensuring...

University of Michigan How to Apply A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and highlight your experiences that directly relate to this position. With questions about the position or office, please email UMSI's Research Office at [email protected] . For requests for accommodations or support with the application process, please email UMSI Human Resources at [email protected] . Who We Are The School of Information is a progressive, interdisciplinary professional school that offers five academic programs. UMSI delivers innovative, elegant and ethical solutions connecting people, information and technology. The school was one of the first iSchools in the nation and is the premier institution studying and using technology to improve human computer interactions. Our school mission is to create and share knowledge so that...

Alkermes, Inc. We are seeking an individual who is talented, motivated, and passionate about science to join our Regulatory Strategy team. As Associate Director of Regulatory Affairs, the successful candidate will play an important role in guiding new products into the clinic and setting the stage for registration. The individual in this role will provide strategic and tactical advice to teams to achieve support the development and maintenance of programs, while ensuring compliance with applicable regulatory requirements. The ideal candidate will have a strong scientific background, and be able to leverage their experience to provide leadership within the department and across R&D. This role reports to the Senior Director, Head of Orexin Regulatory Strategy. Responsibilities Contribute to development of robust, global regulatory strategies for assigned projects. Accountable for adapting and maintaining the regulatory strategy as needed Develop submission plans and...

E.L.F. BEAUTY About the Company e.l.f. Beauty, Inc. stands with every eye, lip, face and paw. Our deep commitment to clean, cruelty free beauty at an incredible value has fueled the success of our flagship brand e.l.f. Cosmetics since 2004 and driven our portfolio expansion. Today, our multi-brand portfolio includes e.l.f. Cosmetics, e.l.f. SKIN, pioneering clean beauty brand Well People, Keys Soulcare, a groundbreaking lifestyle beauty brand created with Alicia Keys, Naturium, high-performance, biocompatible, clinically-effective and accessible skin care, and our newest brand, rhode, a line of curated skincare essentials, formulated for a variety of skin types and needs with high performance ingredients, it's a daily routine that nourishes your skin barrier over time. In our Fiscal year 25, we had net sales of $1 Billion and our business performance has been nothing short of extraordinary with 28 consecutive quarters of net sales growth. We are the #2 mass cosmetics brand in...

Alkermes, Inc. The primary responsibilities of an Associate Director in the Nonclinical Safety Evaluation (NSE) organization are to (1) design and implement nonclinical safety assessment strategies to support the nomination and development of Alkermes' diverse small molecule drug candidates and (2) communicate strategies and findings internally and to regulatory authorities globally. The Associate Director is the single point of accountability within NSE for all strategic, scientific, study-related, and regulatory aspects of the programs he/she manages. The Associate Director in NSE has a broad understanding of toxicology and regulatory requirements to progress candidates through clinical development and is recognized by internal peers for his/her scientific contributions and deliverables (within discipline) to Discovery and Development programs. The individual has specific expertise in one or more areas relevant to nonclinical safety evaluation, shows competency in all aspects,...

Alkermes, Inc. This position is an integral part of the CQA team and provides oversight for and participates in, auditing services in support of Alkermes Clinical Programs by conducting clinical site, vendor qualification, internal systems and document audits to ensure compliance with cGCPs. The CQA Manager supports the department initiatives by leading CQA projects and assists with management of department resources. This position must be able to quickly identify critical and high risk business and compliance issues and report immediately to CQA management and assist/lead investigations and/or corrections of such issues. Travel requirement of 40% - 60% Responsibilities This position will : Schedule, personally conduct and/or supervise Good Clinical Practice (GCP) audit services by an external vendor/consultant and/or internal resources (auditors) which will support Clinical Development activities including but not limited to: Audits of clinical vendors, clinical sites...

Alkermes, Inc. The Associate Director, Regulatory Operations will be responsible for submission management across the development pipeline and support the commercial portfolio. This hands-on position will also assist with regulatory affairs systems, applications, and tools including supporting system implementations, maintenance, updates, and releases. You'll work closely with Regulatory Affairs and cross-functional partners to manage timelines, ensure submission readiness, and strengthen operational excellence across the organization. Key Responsibilities: Lead end-to-end management of regulatory submissions, ensuring timely, compliant, and high-quality deliverables. This role interfaces with external publishing vendor(s) for the preparation of submissions, and internal stakeholders to provide operational oversight and support for eCTD regulatory submission activities. Serve as submission manager and primary contact for publishing vendors and internal stakeholders....

University of Michigan Mission Statement Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society. Job Summary To work with and support licensed veterinary technicians to provide and help coordinate the medical care of research animals within the Unit for Laboratory Animal Medicine (ULAM); to serve as a liaison between the veterinary team, husbandry team, and research laboratory personnel; and to maintain complete and accurate medical records Responsibilities* Perform ongoing medical care for rodents being managed by veterinary technician team through rechecks, including communication with research...

University of Michigan How to Apply A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position. Job Summary The Department of Cell & Developmental Biology is seeking a full-time Research Laboratory Technician Associate in the lab of Dr. Cai, which studies neuronal circuitry and neurogenesis in mouse and fly brains. Responsibilities* We are seeking a motivated and detail-oriented Laboratory Technician Associate to support ongoing research in a collaborative neuroscience laboratory. The successful candidate will contribute to experimental workflows, data analysis, and general laboratory operations. Primary responsibilities include performing routine molecular and cellular biology techniques such as molecular cloning, immunohistochemistry, fluorescence microscopy, and...

Alkermes, Inc. The Executive Medical Director serves as a senior member of the DSPV leadership team, accountable for the management, mentoring and development of assigned benefit-risk management staff as well as serving as a global safety officer for assigned investigational and/or marketed products. Reporting to the Head of DSPV, the Executive Director will also serve in a visible role in providing safety leadership and advisement in several company-wide forums and initiatives. The successful candidate will have demonstrated prior career success as a product safety physician and managing/ developing individuals and highly effective teams. This leader will be expected to roll-up their sleeves and help do the work in addition to managing direct reports. Key success factors also include building high trust, accountability and demonstrating a sense of urgency in leading critical projects, showing the capability to work either independently or collaboratively and to be able to...