- Bristol Myers Squibb (Madison, NJ)
- …leveraging internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role reports to the ... Director of Informed Consent Management. The AD will be responsible for informed consent activities and will also serve as the Global Process Lead for… more
- Pfizer (Pearl River, NY)
- …+ Work closely with other medical monitors to ensure that documents (protocol, Informed Consent Document [ICD], etc.) meet regulatory requirements and company ... country feasibility. **Support study team** + With supervision of medical monitor ( director /Sr director ) provides clinical input to protocol/study team for… more
- Hartford HealthCare (New Britain, CT)
- …to prescribing practices that are safe and evidence based. Obtains appropriate and informed consent for medications trials prior to prescribing. . Acts as ... * Associate Medical Director - General Psychiatry - New Britain, CT* *Hartford HealthCare's Behavioral Health Network (HHC BHN), has* *new opportunity available… more
- ThermoFisher Scientific (Greenville, NC)
- …review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation ... on - now and in the future. **Discover Impactful Work:** The ( Associate ) Medical Director will provide medical support and medical advice for clinical trials and… more
- United Therapeutics (Research Triangle Park, NC)
- …case report forms (CRF) for collection of patient data; Supervise the informed consent composition; Review consultant reports (eg, pharmacokinetics reports); ... in clinical development with a PhD/PharmD + For (Clinical) Product Development Associate Director level: + Master's degree or + 10+ years of product development… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …the diversity and excellence of our academic community. **Description** The Associate Director , Research Projects-School of Medicine, Hematology Medical ... including working with IRB for study approvals, amendments, and writing informed consent and other regulatory documents. + Prior experience in community-engaged… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …core product safety requirements for inclusion in Clinical study protocols (CSPs) and Informed Consent Forms (ICFs), for assigned product(s) + Authors or ... oversees the development of the Safety Management Plan for assigned product(s) + Independently evaluates safety data of any source to identify potential safety signals and performs safety analysis/evaluation. May contribute to safety action recommendations,… more
- Novo Nordisk (Plainsboro, NJ)
- …profile + Develop and update the minimum mandatory safety text (MMST) for use in the Informed Consent + Own the safety sections of the labelling for the evolving ... Committees (ECs) regarding safety aspects of protocols and Patient Information (PI)/ Informed Consent (ICs) + Establish and ensure deliverables to/from Data… more
- CSL Plasma (Las Vegas, NV)
- …to determine a donor's initial and continued suitability for plasmapheresis, explaining informed consent materials to donors. + Performs additional services as ... Usually serves as the primary center physician registered as the Laboratory Director with the Food and Drug Administration (FDA). **Job Description** + Serves… more
- CSL Plasma (Rochester, NY)
- …to determine a donor's initial and continued suitability for plasmapheresis, explaining informed consent materials to donors. 14. Performs additional services as ... Usually serves as the primary center physician registered as the Laboratory Director with the Food and Drug Administration (FDA). Job Description1. Serves as… more
- BrightSpring Health Services (Denton, TX)
- …on quarterly basis for entire contract. CAC approval as needed. + Ensure appropriate informed consent for psych meds and rights restrictions (if needed). + Chart ... team performance though effective leadership, mentoring, and training. + Assists the Executive Director and or Associate Executive Director with timely,… more
- CSL Plasma (Tucson, AZ)
- …to determine a donor's initial and continued suitability for plasmapheresis, explaining informed consent materials to donors. JOB SPECIFICATIONS Provide minimum ... as or delegates to another appropriate physician the duties of "laboratory director ", "technical consultant", or "clinical consultant" as prescribed by the Clinical… more
- AbbVie (South San Francisco, CA)
- …scientific content of Study Protocols, Investigator Brochures, Clinical Study Reports, Informed Consent Forms, briefing documents, charters, and regulatory ... LinkedIn. Job Description In collaboration with a therapeutic area, the Scientific Director , Clinical Science will lead the design, conduct, analysis, and reporting… more
- Pfizer (Pearl River, NY)
- …fit with the clinical program strategy. + Ensure that documents (protocol, Informed Consent Document [ICD], etc.) meet regulatory requirements and company ... Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts with healthcare professionals at sites… more
- Pfizer (Pearl River, NY)
- …clinical program strategy. + Provides oversight to ensure that documents (protocol, Informed Consent Document [ICD], etc.) meet regulatory requirements and ... + Supports Program specific training to study team, investigators, clinical research associate , and others. + Oversees interactions of clinical team with healthcare… more
- CSL Plasma (Loiza, PR)
- …of and apply all rules regarding four-month approvals and grace periods. + Explains Informed Consent to donors, as required by SOP. This includes explanation of ... clear opportunity for donor to refuse participation; obtaining signature and date certifying informed consent . + Handles medical emergencies at the Center by… more
- CSL Plasma (Toa Baja, PR)
- …of and apply all rules regarding four-month approvals and grace periods. 4. Explains Informed Consent to donors, as required by SOP. This includes explanation of ... clear opportunity for donor to refuse participation; obtaining signature and date certifying informed consent . 5. Handles medical emergencies at the Center by… more
- University of Miami (Boca Raton, FL)
- …to explain the purpose of the study and study procedures and obtains informed consent . + Develop and implement strategies for participant recruitment and ... safeguards University assets. Department Specific Functions The Sr. Research Associate 2 will work under the Director ...Research Associate 2 will work under the Director for the Comprehensive Center for Brain Health (CCBH)… more
- Mount Sinai Health System (Elmhurst, NY)
- …pursuant to clinical responsibility, such as arranging follow-up for patients, obtaining informed consent from patients for procedures, recalling patients for ... required professionally or at the request of the supervising physician(s), Director of Service, and/or Supervising Physician Assistant. *-indicates duty is… more
- Mount Sinai Health System (Jamaica, NY)
- …to clinical responsibility, such as arranging follow-up for patients, obtaining informed consent from patients, recalling patients for further evaluation ... required professionally or at the request of the supervising Attending Physician, the Director of Service, and/or Chief Physician Assistant. -The PA may perform the… more