- Parexel (Atlanta, GA)
- …of healthcare industry regulatory compliant data standards. + Good understanding of regulatory requirements & clinical trial design is preferred. **Why ... our team and support the design and execution of clinical trials through advanced analytics and evidence...+ Focus on exploratory work to generate evidence supporting clinical trial design, including outcome summaries and… more
- Parexel (Atlanta, GA)
- …studies, as applicable and/or appropriate for the MD + Providing risk assessment of clinical trials for local sponsorship as needed with the support of the ... papers, slide sets, publications etc. Skills - Experience in clinical medicine (general or specialist qualifications) with...-Experienced as a Physician in Industry or as a clinical trial investigator with significant clinical… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …+ The Regulatory Specialist III is an advanced level position supporting regulatory affairs in clinical trials research. + Employees in this job ... Establishes and maintains processes and monitors practices to ensure regulatory documentation involving clinical trials .... + Leadership and training: May supervise and train Regulatory Specialist I and II staff, lead… more
- Sumitomo Pharma (Atlanta, GA)
- …International Council for Harmonization E6(R2). + Fundamental knowledge of the conduct of clinical trials is preferred. + Strong focus on teamwork, attention to ... our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be...ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure… more
- Bausch + Lomb (Atlanta, GA)
- …plans, ensuring alignment with global requirements. + Provide guidance on risk assessment, clinical trial design implications, and regulatory pathways. + ... optimizing business outcomes. **Responsibilities:** + Formulate, lead, and drive integrated regulatory strategies across CMC and clinical /non- clinical ,… more
- Merck (Atlanta, GA)
- …sound processes, procedures, and strategies for ensuring data integrity in our clinical trials . **Primary Responsibilities:** + Leads their own specific tasks ... Business Processes, Clinical Documentation, Clinical Quality Management, Clinical Systems Implementation, Clinical Trials , Continual Improvement… more
- Veterans Affairs, Veterans Health Administration (Augusta, GA)
- …Patient Safety (HRO-QPS). The incumbent serves as the Chief Health System Specialist Quality and Patient Safety for business and health operations functions within ... HRO-QPS staff under his/her alignment. Responsibilities The Chief Health System Specialist QPS is responsible for the development, enhancement, standardization, and… more
- Veterans Affairs, Veterans Health Administration (Dublin, GA)
- …a consultant for local, network and national programs and/or officials. Manages regulatory affairs and compliance. - Develops and manages program budget and resource ... will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness...is found to be equivalent to a NAACLS-approved US clinical laboratory science degree program. OR The applicant submits… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …plans to each patient's needs and type of cancer; innovative therapies and clinical trials ; comprehensive patient and family support services; and a personalized ... handles administrative activities generally associated with the conduct of clinical trials . The Clinical Research...ADDITIONAL JOB DESCRIPTION: + Serves as the primary oversight specialist on clinical and operational processes for… more
- Parexel (Atlanta, GA)
- …help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory , consulting, and market access, our ... importance of teamwork. **Knowledge And Experience** + Experience in clinical medicine (general or specialist qualifications) with...Experience as a Physician in Industry or as a clinical trial investigator is required + Previous… more
