Associate Director, Clinical QA
Alkermes
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 cGCP and GLP. This person 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. In addition to a travel requirement of ~40%, this person will also need to be onsite and local to our Waltham, MA office 3x a week. Why join Team Alkermes? Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders. We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.
$171k - $236k
...Associate Director, Clinical Science The Associate Director Clinical Scientist contributes to the execution of the clinical development plan for the candidate drug products in collaboration with Project Leaders and Medical Directors. The clinical scientist will be...Suggested$174k - $212k
...disease with well‑understood biology and a clearly defined clinical development and regulatory path, and each expected to provide... ...Position Overview Prime Medicine is seeking an experienced Associate Director of Clinical Data Management to lead clinical data strategy and...SuggestedFull timeTemporary work$161.7k - $202.2k
...Position Summary The Associate Director, Clinical Scientist is a highly collaborative, execution-focused role that supports the development, evaluation, planning and conduct of clinical studies. This position ensures the scientific integrity and accurate interpretation...Suggested- ...Job Summary The Associate Director of Clinical Data Management is a critical position within the ModeX clinical operations team. This position is responsible for successfully leading the execution of all data management activities, ensuring focus on data integrity, validity...Suggested
$174k - $212k
Prime Medicine is seeking an Associate Director of Clinical Data Management in Watertown, MA. This role involves leading clinical data strategy and execution for gene editing. The ideal candidate will have extensive experience in clinical trials and vendor oversight. The...Suggested- Prime Medicine in Watertown, MA, is seeking an Associate Director, Clinical Data Management to drive clinical data strategies for gene editing programs. The candidate will lead internal and external data management activities crucial for IND, CTA, and BLA submissions....
$176.1k - $287.3k
...This role provides an exciting opportunity to lead projects across diverse therapeutic areas. As the Associate Director, Clinical Diagnostics (CDx), you will own the end-to-end strategy, development, and lifecycle management of companion diagnostic solutions that enable...$160k - $240k
Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to...Full timeContract work- ...will inspire you and empower you to shine? Join us as an Associate Medical Director in our Neuroscience Therapeutic Area Unit in our Cambridge... ...Associate Medical Director leads and drives strategy for clinical studies within the overall global clinical development for...Work at officeRemote workNight shift
- ## Associate Director, Clinical ScientistApplyremote type: Site Basedlocations: South Boston, MAtime type: Full timeposted on: Posted 11 Days Agojob requisition id: R-100056**Job Description:****Company Overview**Founded over a decade ago, CRISPR Therapeutics is a leading...Remote work
$154.4k - $242.55k
...employment application is true to the best of my knowledge. Job Description Objective / Purpose: The Supply Chain Management, Associate Director is responsible for managing and optimizing various aspects of the supply chain process. This role involves developing and...Minimum wageFull timeTemporary workLocal areaWorldwide$170k - $190k
About Jade Biosciences Jade Biosciences is a clinical‑stage biotechnology company focused on developing best‑in‑class therapies that... ....com and follow the Company on LinkedIn. Role Overview The Associate Director, Clinical Site Budgets & Payments will architect and lead...Contract workRemote work$211.91k - $256.79k
Associate Director, Global Clinical Science Reports through the Clinical Development function which provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective Responsible for implementation, planning, and...Hourly payFull timeTemporary workSummer workFlexible hoursShift work$160.8k - $201k
About the Role The Associate Director, Quantitative Clinical Pharmacology is responsible for providing translational, clinical pharmacology, and pharmacometrics deliverables for development assets from pre‑IND to Phase III. The incumbent will apply quantitative modeling...$211.91k - $256.79k
Myana is seeking an Associate Director for Global Clinical Science to lead implementation and execution of clinical trials. This role demands thorough protocol understanding, skilled collaboration with cross-functional teams, and scientific leadership in delivering high...- Vertex Pharmaceuticals is seeking a Clinical Study Quality Lead, Associate Director in Boston to oversee advanced quality assurance in clinical trials. Responsibilities include managing compliance with GCP standards, risk management, and coordinating with multiple stakeholders...
- ...and effectively manages and communicates multi-disciplinary Clinical Pharmacology development plans and strategies that achieve commercial... ...position can be hired based on the below qualifications: Associate Director, Clinical Pharmacology PhD with typically 4+ years of...Full timeLocal area
$200k - $240k
...Associate Director, Clinical Supply Chain At Merida Biosciences, we are pioneering true precision medicines for antibody-driven diseases. We specifically target pathogenic antibodies and their cellular sources with bespoke Fc biotherapeutics engineered to selectively...Local area- ...Associate Director, Clinical Scientist, Internal Medicine At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director to join our Clinical Scientist, Internal Medicine team supporting...Worldwide
$187.5k - $254k
...Associate Director/Medical Director, Clinical Development Climb Bio is a clinical-stage biotechnology company developing therapeutics for patients with immune-mediated diseases. Our product candidates include budoprutug, an anti-CD19 monoclonal antibody that presents...Work at officeLocal area$142.4k - $224.1k
...responsible and accountable for the successful execution of the clinical data management strategy for one or more drug or vaccine... ...experience working with formal project management tools and processes Associates Degree with at least 7 years’ professional experience in...For contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$148k - $236.5k
Pioneering Medicines: Associate Director / Director, Clinical Operations Cambridge, MA USA What if... We could harness the power of Flagship’s scientific platforms and create novel treatment options that benefit more patients, sooner? Pioneering Medicines, an initiative...For contractors- Takeda is seeking an Associate Medical Director in Cambridge, MA to lead strategy for clinical studies within the Neuroscience Therapeutic Area. This role involves collaboration with global teams and decision-making impacting regulatory approvals. The ideal candidate holds...
$101k - $151.5k
...We have more than 6,400 employees and associates in our partner dental practices and operate... ...week. The Opportunity The Associate Director, Clinical Services leads a team of Registered... ...avoidable costs. Monitor Quality Assurance (QA) reviews regularly and provide staff...Work at officeLocal area2 days per week$273.21k - $331.06k
Functional Area Description The Associate Director, Global Clinical Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy,...Hourly payFull timeTemporary workPart timeSummer workFlexible hours- Regeneron Pharmaceuticals, Inc seeks an Associate Director for their Clinical Scientist team focused on Ophthalmology. The role involves contributing to clinical studies' development and execution while ensuring scientific integrity. Candidates should have over 10 years...
$160k - $195k
...address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic... ...follow us on X, LinkedIn and Facebook. Role Summary: The Associate Director, Quality Management Systems is a key member of the quality...Local area- Target PR Range: 113-160/hr Summary of Position Looking for an associate or director-level subject matter expert to build clinical operations compliance while upholding our core values and staying true to our mission. Reporting to the Head of Clinical Operations, the Director...Work at officeFlexible hours
- Orro is seeking a Supply Chain Manager in Cambridge, MA to oversee the strategic and operational management of clinical supply activities. This role requires expertise in supply chain strategy and vendor oversight while ensuring compliance with regulations. The ideal candidate...Flexible hours
- Responsibilities Lead the strategic and operational management of complex clinical supply activities across all phases of development Collaborate with Clinical Operations/Development, Quality, Regulatory Affairs, and external partners to manage supply planning, inventory...
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