- Novo Nordisk Inc. (Plainsboro, NJ)
- …evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We're changing lives for a living. Are you ready to make a ... difference? The Position The Assoc Director OED - Supplies, is responsible for US and...with all relevant regulations and policies; (Good Clinical Practice ( GCP ), ICH guidelines, federal regulations (Sunshine/Open Payments Act), and… more
- Eisai, Inc (NJ)
- …If this is your profile, we want to hear from you. Job Summary The Associate Director , Clinical Outsourcing, will oversee and lead and support activities related ... development.#LI-TS1Eisai Salary Transparency Language:The base salary range for the Associate Director , Clinical Outsourcing is from :157,200-206,300Under… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …equal opportunity employer including veterans and people with disabilities. Summary The Associate Director , External Data Management, is accountable for the ... on behalf of Daiichi Sankyo. This position also ensures quality delivery of all 3rd party data from diverse...implement best practices across the Clinical Trial lifecycle. Applies GCP principles to ensure all external data management activities… more
- Novo Nordisk (Lexington, MA)
- …before, during and after inspections, working with stakeholders across multiple functions. The Associate Director , CQ, R&D Quality - will also act as ... for patients. Do you dream of using your solid GCP knowledge, process optimisation skills and quality ...a member of our team and serve as an Associate Directors for Clinical Compliance, Research & Development (R&D)… more
- Kelly Services (Burlington, MA)
- **Sr. Manager/ Associate Director - Quality ... function. This individual will report to the Sr. Director of Global GCP /GLP compliance and while ... They will play a key role in expanding and shaping US-based Quality culture, including GCP and GLP compliant business units. This is a full-time, onsite… more
- Merck (Columbus, OH)
- …level sites that require headquarters input. Other Responsibilities + Provides input into GCP Quality and Compliance Council regarding the Quality Management ... new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific… more
- Frontier Medicines (Boston, MA)
- Join us as the Senior Manager/ Associate Director of Quality Assurance at Frontier, where precision meets purpose. In this pivotal role, you'll oversee GCP ... head of RA/QA as we navigate the complexities of quality assurance with precision and purpose. Requirements What will...not limited to: US CFR, EU CTD, and ICH GCP + Familiarity with electronic document management systems and… more
- GRAIL (Durham, NC)
- …partnerships with pharmaceutical companies for companion diagnostic (CDx) tests. The Associate Director will work cross-functionally to manage Grail's Clinical ... 14155, IVDD/IVDR), US [21 CFR Part 812 and Part 11]. + Experience managing GCP quality processes such as managing Quality Events and CAPAs; and participating… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- We are seeking a Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the ... of study data of a clinical development program. The Associate Director leads in a matrix environment...maintaining compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical… more
- Amicus Therapeutics (Princeton, NJ)
- Associate Director , Clinical Data Management Location Princeton, NJ Requisition ID 2245 # of openings 1 Apply Now ... (https://phh.tbe.taleo.net/phh04/ats/careers/v2/applyRequisition?org=AMICUS&cws=37&rid=1289) Associate Director , Clinical Data Management Amicus Therapeutics is… more
- ThermoFisher Scientific (Las Vegas, NV)
- …find cures for cancer. Due to continued growth, we are looking to appoint an Associate Medical Director at the Las Vegas Clinical Research Unit. This role is ... an office-based position for a motivated Physician. The Associate Medical Director serves as the physician...being conducted under all applicable laws, regulations and per ICH- GCP guidelines in the organization's Clinical Research Unit (CRU).… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …therapeutic area preferred, along with relevant industry experience. A minium of 2-3yr ( Associate Director ), 4-8yr ( Director ) prior industry experience or ... The Associate Medical Director works with their...trial execution, reviewing adverse events, monitoring patient health, and quality of results * Analyzes the benefits and risk… more
- AbbVie (North Chicago, IL)
- …implement translational strategies to advance AbbVie's innovative Oncology pipeline. The Associate Director , Biomarker Program Management, leads a team within ... quality and efficiency, on-time, within budget, and meet objectives. The Associate Director achieves these objectives via scientific expertise, strategic… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Associate Director , Medical Coding, Analytics & Process is responsible for ... develop, and maintain metrics and algorithms to measure coding quality and support quality review. The incumbent...+ Firm knowledge of regulatory environment in Pharmacovigilance and GCP . + Experience with clinical trial databases and/or PV… more
- Gilead Sciences, Inc. (Seattle, WA)
- …impact. Join Gilead and help create possible, together. **Job Description** The Associate Director , Clinical Records & Information Management will partner with ... and Functional Service Provider (FSP) to ensure timely and quality delivery of the TMF. This role is a...file in pharmaceutical/biotechnology industry. + Excellent working knowledge of GCP regulations. + Direct experience with Veeva Clinical Vault… more
- BeiGene (Emeryville, CA)
- The Associate Director (AD) Clinical Study Management leads both indirect and direct reports, external partners, consultants, vendors and external budget to ... effective communication and collaboration with functional area peers including Drug Safety, Quality Assurance and Regulatory Affairs, as well as thought leaders in… more
- University of Rochester (Rochester, NY)
- …Services Unity (CMSU), consisting of approximately 15 team members, with two Directors ( Director Operations and Director Quality Assurance) and the clinical ... organizations 2. Oversee all aspects of operations, including operations, quality assurance, facilities, finance and administration, project prioritization, resource… more
- Novo Nordisk (Lexington, MA)
- …to develop new medicines for patients. The Position We are looking to hire an Associate Director of Clinical Operations. This is a unique opportunity to work in ... merges biotech speed and agility with large pharmaceutical company quality , resources , and stability, uniting the best of...phases of research + Strong knowledge of ICH guidelines, GCP and FDA regulations + Experience with all aspects… more
- Bristol Myers Squibb (Minneapolis, MN)
- …and spirit of independence and love of challenge._ **Job Description** The Region Director (RD) is a remote leadership position that is primarily responsible for ... satisfaction and productivity. This position reports into a national Field Medical Director role. The RD position is underpinned with the expectation of leadership… more
- IQVIA (Durham, NC)
- …on continuous learning and career development. **Purpose:** To assist the department Director in developing department strategy and team building; to ensure a high ... facilitate escalation management. **RESPONSIBILITIES:** + Ensure consistent and outstanding quality against department deliverables. + Manage customer relationships and… more
