- Olema Oncology (San Francisco, CA)
- …patients feel better, longer. For more information, visit us at www.olema.com. About the Role Associate Director , GMP Quality Assurance As the Associate ... Metrics for product quality and compliance Partner with GCP Quality Assurance and Pharmacovigilance to ensure compliance with international regulations… more
- Sumitomo Pharma (Pierre, SD)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Medical Director .** The Associate Medical Director ... (SmPC), and Canadian Product Monograph (PM) + Ensures timely and quality review and assessment of ICSRs, including seriousness, expectedness, safety narratives,… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ... functional compliance teams for regulations impacting Clinical, Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and procedures and… more
- BeOne Medicines (San Mateo, CA)
- **General Description:** _The Associate Director , Safety Scientist supports assigned compounds in conjunction with Product Safety Leads (PSLs) and leverages ... in departmental activities **Supervisory Responsibilities:** This position has no direct reports. The Associate Director , Safety Scientist is part of a team that… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ... Quality team and share insights to trends to Clinical Pharmacovigilance and Medical Quality and R&D Quality leadership for proactive risk mitigation and… more
- System One (Tarrytown, NY)
- Job Title : Temp - Associate Director , Aggregate Reporting, GPS Type: Contract Compensation: $85 - $100 hourly (dependent on experience) Contractor Work Model: ... Remote Highlights should include: 1. Pharmacovigilance & Aggregate Reporting Expertise + Direct experience authoring...interpret clinical data to support benefit-risk assessments. Temp - Associate Director , Aggregate Reporting, GPS + Submit… more
- ThermoFisher Scientific (Wilmington, NC)
- …services. Work related travel 10-20% possible. **Discover Impactful Work:** The Associate /Medical Director provides medical oversight of clinical trials to ... digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities… more
- Takeda Pharmaceuticals (Boston, MA)
- …for CPMQ activities eg audit, inspection, QE, CAPA. + Organise Clinical and Pharmacovigilance Quality council meetings and proactively manage the agenda and ... of my knowledge. **Job Description** **OBJECTIVES:** + Ensures Global and R&D Quality processes are embedded and effectively implemented across CPMQ + Partner with… more
- AbbVie (North Chicago, IL)
- …data and insights to the forefront of decision making via fit-for-purpose solutions. The Associate Director , RBQM Analytics in Data Science and Analytics is a ... data sources (biomarker/translational, big data, digital sources, real world data, pharmacovigilance data, clinical trial data) . Responsible for coaching, mentoring… more
- AbbVie (North Chicago, IL)
- …and insights to the forefront of decision making via fit-for-purpose solutions. The Associate Director , Medical Monitoring Analytics is a leadership role and is ... data sources (biomarker/translational, big data, digital sources, real world data, pharmacovigilance data, clinical trial data) + Responsible for coaching, mentoring… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director , Affordability COE PB - Call Center in Patient Support Services **Location** : Cambridge, MA Morristown, NJ **About the Job** ... to field teams that provide education and support to patients and customers. As the Associate Director of Affordability - Call Center - in the newly formed… more
- Regeneron Pharmaceuticals (Armonk, NY)
- The Associate Director , Global Development Quality Inspection Management (GDQIM) acting as an Inspection Management Lead (IML) is a key position that is ... and/or Investigator Site Preparation Visits, in collaboration with the GD Quality Assurance (GDQA) team and other relevant functional groups. * Identifying… more
- Organon & Co. (Plymouth Meeting, PA)
- …improve the lives of women globally. We are looking for an experienced Associate Director , Program Management to join our team. This successful candidate ... and accurate program information in reports and systems to enable high quality portfolio communications. + Contribute to and facilitate an environment that fosters… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …research through post-marketing + Strong experience in Good Clinical and Good Pharmacovigilance Practices and knowledge of evolving regulations, such as ICH E6 R3 ... Proven experience advising business functions in the biopharma industry on quality and compliance requirements and continuous improvement + Experience working across… more
- AbbVie (South San Francisco, CA)
- …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Medical Director leads the direction, planning, execution, and interpretation of clinical ... and may lead cross-functional teams to generate, deliver, and disseminate high- quality clinical data supporting overall product scientific and business strategy.… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Specialized Pharmacist or Master of Drug Regulatory Affairs, RAC certification preferred ** Associate Director Experience Requirements:** + Two (2) years of ... professional experience in a scientific, clinical, and/or medical space. **Sr. Associate Director Requirements:** + Five (5) years of professional experience in… more
- J&J Family of Companies (Spring House, PA)
- …impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Quality **Job Sub** **Function:** Clinical Quality **Job Category:** Professional ... The **Specialist, Early Development Risk Management,** reports to the Director , Early Development Clinical Risk Management. The Specialist Early Development… more
- University of Maryland, Baltimore (Baltimore, MD)
- …of Pharmaceutical Sciences with teaching responsibility to the Graduate Program Director and Associate Dean for Graduate Programs. *_ACADEMIC RESPONSBILITIES ... science, including: Chemistry, Manufacturing, and Controls (CMC); Clinical Research; Pharmacovigilance ; Phase IV Research (eg, Pharmacoepidemiology); and Drug and… more
