Clinical Quality & Compliance Associate Director
Stoke Therapeutics
Stoke Therapeutics seeks an Associate Director, Clinical Quality Compliance to serve as a primary GCP/GCLP quality contact. Reporting to the VP of Quality, this role partners with Clinical Development, Regulatory, and others to ensure global compliance and drive inspection readiness across Stoke’s clinical and bioanalytical studies. The role requires leading inspection prep, CAPA management, risk-based quality plans, and collaboration across functional teams to mature Stoke’s quality culture and #J-18808-Ljbffr Stoke Therapeutics
$192k - $215k
...approach. Stoke is headquartered inBedford, Massachusetts. For more information, visit Position Purpose: The Associate Director, Clinical Quality Compliance will be a primary quality contact for GCP and GCLP compliance. This role will report into The VP of Quality and...SuggestedTemporary work$176.1k - $287.3k
...We are seeking a highly motivated Associate Director (AD) to join the Quantitative Pharmacology... ...strategies in partnership with Clinical Pharmacology, Biostatistics,... ...documentation are of the highest scientific quality and regulatory compliance.This role requires:PhD in...SuggestedFull timeRemote work$182k - $199k
...is seeking an experienced and driven Associate Director, Clinical Supply Chain to lead the planning, forecasting... ...with Clinical Operations, Quality, Regulatory, Manufacturing, and external... ...strategy while ensuring regulatory compliance. The role plays a critical part in managing...SuggestedTemporary workRemote work$243.6k - $329.4k
...for people with serious diseases. We are seeking a Medical Director, Clinical Development to join our Clinical Development Program (CDP) team... ...Head, and Strategic Program Teams to deliver high-quality, scientifically sound program milestones. This position offers...SuggestedFull timeWorldwide$176.1k - $287.3k
...medicines for people with serious diseases. We are seeking an Associate Director to join our Clinical Scientist, Internal Medicine team supporting... ...supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional...SuggestedFull timeWorldwide$109.9k - $179.3k
...Affairs Strategy (Oncology) team.The Associate Manager, Regulatory Affairs will... ...development of novel therapeutics including quality, preclinical and clinical areas of drug development and the... .../procedures required to ensure compliance with regulations.This position...Full timeWorldwide$154.8k - $252.8k
The Associate Director, Precision Medicine Clinical Laboratory Operations will be responsible for Clinical Laboratory Project & Program management for various therapeutic areas working closely with Director, Precision Medicine Clinical Laboratory Operations and key cross...Local area- Boehringer Ingelheim is seeking an Associate Director Lead or Senior Associate Director Lead in Clinical Pharmacology at the Ridgefield, CT site. Roles involve designing CP development strategies, PK/PD assessments, and regulatory interactions to support from early development...
$176.1k - $287.3k
Associate Director of Pathology has primary responsibility to support drug molecule efficacy and safety studies in a variety of therapeutic... ...focus areas (TFAs). The successful candidate will also provide Clinical Pathology support for GLP toxicology and PK studies of...Full time$243.6k - $329.4k
...for people with serious diseases. We are seeking a Medical Director, Clinical Development to join our Clinical Development Program (CDP) team... ...Head, and Strategic Program Teams to deliver high-quality, scientifically sound program milestones. This position offers...Worldwide$140k - $222k
...during the interview process. Boehringer Ingelheim is currently seeking a talented and innovative Associate Director Lead or Senior Associate Director Lead to join our Clinical Pharmacology department located at our Ridgefield, CT facility. The Associate Director,...Local areaRemote workRelocationFlexible hours2 days per week3 days per week- ...Excellent employment opportunity for a Compliance Specialist in the Ridgefield, CT area.... ...operational duties to support the Medical Affairs Quality Manager, including development of... ...A plus, knowledge regarding Pharma Clinical Trial processes and inspection readiness...Contract work
$176.1k - $287.3k
...together: We're seeking an Associate Director to lead companion... ...biomarker feasibility through clinical validation, regulatory submission... ...scope, timelines, and quality expectations. Support global... ...alignment. Ensure compliance with relevant standards (ISO...$176.1k - $287.3k
The Associate Director of Translational/Preclinical Modeling develops and implements quantitative and mechanistic PK/PD models to aid in the... ...modality selection/optimization, and contributes to early clinical trial dose selection and/or design and advancement and strategic...Full time$176.1k - $287.3k
...qualified statistician/biostatistician to support Clinical Biostatistics with Global Development. In this... ...in representing the company in professional associations, conferences, and publications. As an Associate Director, the incumbent will be responsible for mentoring...Full time$176.1k - $287.3k
Build Our Future TogetherThe Associate Director role involves supporting Pharmacokinetics (PK) and Pharmacokinetics/Pharmacodynamics (PK/PD... ...preclinical studies.Working closely with Toxicology, Pathology, Clinical Pharmacology, and Quantitative Pharmacology teams within the...Full time$157.2k - $256.6k
...people with serious diseases. We are seeking an Associate Director to join our Regeneron Genetic Medicines Clinical Development Unit (RGM CDU). The Associate Director... ...a high-performing, strategic, effective, and quality-focused organization that is well-aligned and integrated...Permanent employmentFull timeContract workWorldwide$176.1k - $287.3k
...medicines for people with serious diseases. We are seeking an Associate Director to join our Clinical Scientist, Internal Medicine team supporting... ...supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional...Worldwide- ...projects simultaneously, and meet deadlines in a fast-paced, dynamic environment. Detail-oriented mindset with a focus on quality, accuracy, and compliance. Experience with regulatory submissions for small molecules, biologics, or other pharmaceutical modalities is...
$176.1k - $287.3k
Associate Director Pharmacometrics Programming provides timely support to the study team on all programming... ...processing/analyzing/storing data from clinical studies according to a Statistical... ...study team to provide timely and quality support for analysis and reporting of clinical...Full time$176.1k - $287.3k
...Associate Director (Peptidomimetics), R&D Chemistry We are currently seeking an established leader and drug hunter for the R&D (Research & Development... ...therapeutics (i.e., advancement of molecules into the clinic) with experience building and leading teams is required....Temporary work$154.8k - $252.8k
...serious diseases. We are seeking an Associate Director to join our Clinical Data Management team.As an... ...processes, and the delivery of high-quality, compliant external data from third... ...Specification (DTS) documents to ensure compliance with Regeneron standards and timelinesProviding...Full timeWorldwide$183.1k - $305.2k
...life-changing medicines for people with serious diseases. Our Global Patient Safety (GPS) organization is seeking a Director, GPS Quality & Compliance to support our quality event management and inspection readiness programs. This role partners closely with the Senior...Full timeWork at officeWorldwide$250k - $394k
...abreast of paradigm shifts in clinical practice, and aligns with BI... ...Affairs Strategy Executive Director to ensure seamless... ...content, and develops and tracks associated measurable business outcomes... ..., customer focus and ensure compliance standards are met. Leverages...RelocationShift workNight shift$104.5k - $156k
Join to apply for the Associate Medical Director role at Optum 1 day ago Be among the first 25 applicants... ...everyone. At Optum, you’ll have the clinical resources, data and support of a... ...models focused on managing risk, higher quality outcomes and driving change through...Minimum wagePart timeWork experience placementLocal areaRemote workWork from homeAfternoon shiftEarly shift$176.1k - $287.3k
...therapeutics. You will collaborate with various RGC teams and with pre-clinical and clinical development teams at Regeneron to catalyze... ...from longitudinal clinical data, design and execute genetic association studies, and perform integrative omics analyses to address these...$157.2k - $256.6k
...Build our future together: The Associate Director of HCP Marketing will lead healthcare professional marketing strategy and execution for... ...Affairs, TLLs, Market Research, Market Access, Regulatory, Legal, Clinical, and HEOR to deliver cohesive, compliant, and impactful...Work at office$173.5k - $283.1k
...Regeneron Pharmaceuticals is seeking an Associate Director, Diagnostics Project Management &... ...This leadership role within Regeneron's clinical diagnostics team provides portfolio management... ...the Diagnostics function to ensure quality, efficient and timely delivery. Effectively...$205k - $341.6k
...serious diseases. We are seeking a Director to join our Regulatory... ...will be actively involved in clinical study support and will lead IND... ...requirements.Ensuring the quality and timeliness of regulatory... ...from other functions to ensure compliance and alignment with project timelines...Full timeWorldwideRelocation package$200k - $316k
...Description Ensure strategic HEOR and healthcare quality management of one or more therapeutic... ...strategic plan that translates complex clinical data into a coherent value narrative... ...quality deliverables, timeliness, and compliance to budget. Provide day-to-day guidance on...Remote jobLocal areaRelocation
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