- GRAIL (Durham, NC)
- …GCP audit program SOPs and templates, ensuring they remain current with evolving regulatory requirements and industry best practices. + Review and provide ... partnerships with pharmaceutical companies for companion diagnostic (CDx) tests. The Associate Director, Clinical Compliance will play a key leadership role in… more
- First Horizon Bank (Charlotte, NC)
- …on site in Nashville, TN & Charlotte, NC. The HR Risk & Associate Relations Director is a strategic leadership role responsible for protecting the organization's ... talent and reputation by proactively managing HR compliance, risk, fraud, and associate relations. This role advances business priorities by cultivating a culture of… more
- ThermoFisher Scientific (Wilmington, NC)
- …trials, oversee case-processing activities through all phases of development and perform regulatory reporting and medical monitoring. As part of your work with ... and oversight of all contracted services. **Discover Impactful Work:** The Associate /Medical Director provides medical oversight of clinical trials to ensure company… more
- Regions Bank (Charlotte, NC)
- …credit risk review procedures, sound lending practices, credit policies, and regulatory requirements + May offer advice and guidance to junior examiners where ... law. Such information will be stored in accordance with regulatory requirements and in conjunction with Regions' Retention Schedule...Schedule for a minimum of three years. You may review , modify, or update your information by visiting and… more
- Pfizer (Sanford, NC)
- …or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to ... work. **What You Will Achieve** In this role, you will: + Evaluate, review , and approve validation master plans, protocols, and reports, ensuring compliance with … more
- Pfizer (Sanford, NC)
- …or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to ... In this role, you will: + Perform batch record review and final batch disposition for clinical and commercial...site. + Complete queries for batch data to support regulatory requests. + Contribute to APRs for batch release… more
- Sumitomo Pharma (Raleigh, NC)
- …a dynamic, highly motivated, and experienced individual for the position of ** Associate Medical Director.** The Associate Medical Director will provide hands-on ... and Canadian Product Monograph (PM) + Ensures timely and quality review and assessment of ICSRs, including seriousness, expectedness, safety narratives, adverse… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- **Job Summary** **** The Associate Director, MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing processes ... aspects of downstream process technology transfers to CDMOs, including documentation review , gap analysis, and risk assessment. + Provide expert technical oversight… more
- Wells Fargo (Charlotte, NC)
- …this role:** Wells Fargo Advisors (WFA) is seeking a Supervisory Control Associate responsible for direct support of branches and their responsibilities for remote ... Private Client Groups + Perform basic or tactical ongoing regulatory , compliance and operational reviews as well as other...background standards. Wells Fargo will initiate the FINRA licensing review process at the time of offer acceptance. For… more
- Grifols Shared Services North America, Inc (Goldsboro, NC)
- …solutions and services in more than 110 countries and regions. **Quality Systems Associate ** ** ** **Summary:** Under the direct supervision of the Quality Systems ... in the chart below):** ** ** * Completes weekly review of equipment QC and maintenance records. * Documents,...Systems Manager to ensure that cGMP regulation, SOPs and regulatory requirements are followed. Duties include: Under the direct… more