- Insmed Incorporated (San Diego, CA)
- …strategic direction with cross functional working groups to identify and mitigate GCP quality and compliance issues.Supports the evaluation and acceptability of ... for Millennials™, and Best Medium Workplaces™ lists.OverviewReporting to the Executive Director of Clinical Quality Assurance, the Director of Clinical… more
- Merck & Co. (San Antonio, TX)
- Job DescriptionRole SummaryThe Regional Medical Scientific Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in ... questions about Company products. The work of an Regional Medical Scientific Director is aligned to: Scientific Exchange, Research, Scientific Congress Support, and… more
- Merck & Co. (Chicago, IL)
- …DescriptionWe are seeking a Growth and Improvement minded Regional Medical Scientific Director (Medical Science Liaison / MSL) - in Inflammatory Bowel Disease ... our Strategic Operating Priorities.Summary, Focus and PurposeThe Regional Medical Scientific Director (Medical Science Liaison) is a credentialed (ie, PhD, PharmD,… more
- Merck & Co. (North Wales, PA)
- …the ability to:--Strong knowledge of clinical research regulatory requirements (eg, GCP and ICH) Proven ability to manage competing priorities and effectively ... consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents… more
- Merck & Co. (Rahway, NJ)
- …- Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices ( GCP ) is highly desirable. - Preferred Experience and Skills: - - Proficiency ... consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents… more
- Eisai, Inc (Nutley, NJ)
- …of the Quality management system. This role is responsible for Good Clinical Practice ( GCP ) oversight, and for assuring the compliance of projects, products and ... a difference. If this is your profile, we want to hear from you. Director , Clinical Quality Assurance The Director , Clinical Quality Assurance position is… more
- Twist BioScience (South San Francisco, CA)
- Sr. Director , Manufacturing Execution System (MES) (Hybrid in South San Francisco)Job DescriptionWe are seeking an experienced and highly motivated Manufacturing ... Execution System (MES) Director to lead the strategic development, implementation, and optimization of our custom, in-house developed MES solutions across our… more
- Merck & Co. (North Wales, PA)
- …data/medical protocol deviations in collaborations with the Clinical Director .Other responsibilities include:Collaborating cross-functionally in the development of ... the ability to:Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to manage multiple competing priorities with good planning,… more
- Merck & Co. (Rahway, NJ)
- …data/medical protocol deviations in collaborations with the Clinical Director . Other responsibilities include: Collaborating cross-functionally in the development ... clinical research regulatory requirements (e . g . , GCP and ICH) Ability to manage multi e competing...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Clinical Dynamix, Inc. (Watertown, MA)
- …ensuring adherence to contractual agreements, timelines and quality standards Ensure compliance with regulatory requirements, ICH- GCP requirements, and company ... MA is expanding for their high profile clinical development trials. The Director , Clinical Operations is a leadership role responsible for overseeing and managing… more
- Palo Alto Networks (New York, NY)
- …- just to name a few! Job Description Your Career As a Senior Consulting Director within Unit 42's Cyber Risk Management (CRM) team, you will lead our Cloud Security ... and thought leadership, and advancing service innovation. Working closely with the Managing Director and CRM NAM Practice leader, along with peers in North America… more
- Teva Pharmaceuticals (West Chester, PA)
- …make a difference with. The opportunity We are seeking an experienced Sr. Director , GCO Therapeutic Area Head to lead the strategic and operational global execution ... and CROs, ensuring that vendor responsibilities such as performance, quality & compliance , and reporting are met Accountable for the performance and results of… more
- Alkeus Pharmaceuticals (Cambridge, MA)
- …and in compliance with quality and regulatory standards. The Associate Director plays a critical role in planning, assessing feasibility, activating sites, as ... of blindness in the US Position Summary: The Associate Director is responsible for leading and managing global, late-stage...adhere to applicable global regulatory and ethical standards (ie GCP , ICH, ) to support audit readiness and safeguard… more
- Neurocrine Biosciences, Inc. (San Diego, CA)
- …Facebook. (*in collaboration with AbbVie) About the Role: The Executive Medical Director will be primarily responsible for developing and executing the Neurology ... of clinical development projects globally to achieve company objectives in compliance with GXP and regulatory requirements Create and foster strong relationships… more
- Arrowhead Pharmaceuticals (Verona, WI)
- …as ICH/FDA guidance documents, including experience with development of applicable compliance programs. Knowledge of GLP/ GCP regulations Understanding of ... need. The Position The purpose of this position within the Quality and Compliance department is to lead Quality Control (QC) Laboratory consisting of analytical,… more
- Barrington James (Madison, OH)
- …and participate in interactions with global health authorities as needed. Ensure compliance with GCP , ICH, and applicable regulatory guidelines. Stakeholder ... Medical Director , Clinical Development (Oncology) Location: US Remote A...trials and working with cross-functional teams. Solid knowledge of GCP , ICH, and global regulatory requirements (FDA, EMA). Excellent… more
- BioSpace (New York, NY)
- …the implementation of risk-based monitoring strategies, as applicable, while ensuring protocol compliance and subject safety. They will play a critical role in ... assigned clinical trials, ensuring quality site monitoring in accordance with GCP , protocol, and regulatory requirements. Perform oversight and co-monitoring visits,… more
- Torrey Pines Solutions (San Francisco, CA)
- About the job Associate Director , Clinical Operations Key Responsibilities * Team Management - Provide leadership and direction to Clinical Program Leads : *Recruit, ... *Support regulatory authority and Sponsor audits and inspections. *Escalate compliance issues/risks to Clinical Operations, Medical and biopharma leadership. *Create… more
- Alira Health (Framingham, MA)
- …strategies for sites. Maintains regular contact with study sites to ensure protocol/ GCP compliance , assesses patient accrual rates, and responds to sponsor ... for clinical trials. CRAs work closely with the In-house CRAs, Lead CRAs, Director of Clinical Monitoring and Project Managers to ensure sites' protocol … more
- NYULMC (New York, NY)
- …trial while maintaining the fidelity of the clinical research protocol and compliance with policies, procedures and regulations. The oncology clinical research nurse ... the first year of the position including but not limited to comprehension and compliance with all NYU PCC Clinical Trials Office policies and procedures, NYU OSR and… more
