- Beth Israel Lahey Health (Burlington, MA)
- …general research duties. Implements study protocols in accordance to regulatory and institutional requirements. Works closely with principal investigators, research ... research SOPs, FDA, OHRP, and GCP regulations. + Immediately develops coordinator /sponsor relationship. + Completes start- up checklists and organizes study start-up… more
- Carle Health (Champaign, IL)
- Overview The Strategic Planning Coord II is responsible for guiding the organization's strategic planning process through market analysis, service line strategic ... Conducts internal and external assessments, prepares business/strategic plans, and manages regulatory activities in conjunction with service line leaders and project… more
- US Tech Solutions (North Chicago, IL)
- …3. **Contractual or Paralegal** experience highly preferred **Purpose:** The Contract Coordinator in **R&D Procurement** will be responsible for timely and ... Ability to learn multiple concepts related to legal, compliance and regulatory matters in Clinical Research Experience in cross-functional interactions and working… more
- McLaren Health Care (Detroit, MI)
- **Job Summary:** Provide study coordinator /data management/ regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, ... providing excellent customer support and guidance in the clinical trials arena. **Responsibilities:** + Assure all study requirements are met and documented and meet both internal and external regulations in accordance with protocol guidelines. + Maintain… more
- Mount Sinai Health System (New York, NY)
- …subject data through chart reviews. + Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, ... the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, and for studies involving… more
- Seattle Children's (Seattle, WA)
- …are looking for a highly motivated and well-organized **Clinical Research Coordinator Level 2** who possesses **proven experience** in coordinating **multicenter ... **single IRB** processes and ensuring meticulous adherence to **all relevant regulatory compliance** requirements, with a strong ability to **deliver by established… more
- US Tech Solutions (North Chicago, IL)
- **Purpose:** The Contract Coordinator in **R&D Procurement** will be responsible for timely and appropriate **integration of agreements** including creating ... Ability to learn multiple concepts related to legal, compliance and regulatory matters in Clinical Research Experience in cross-functional interactions and working… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and ... resolution of data queries. + Prepare and or complete regulatory related reports and IRB submissions. Maintain and organize...related reports and IRB submissions. Maintain and organize study regulatory binders, enter all required study data on an… more
- ThermoFisher Scientific (Tucson, AZ)
- …customers, patients and healthcare providers. We engage with healthcare professionals, regulatory agencies and pharmaceutical customers to help them navigate ... regulatory and compliance requirements around the world. We manage...inquiries and documents interactions according to organizational, client and regulatory guidelines. The information provided will be given to… more
- Centene Corporation (Westmont, IL)
- …resolve issues and documents member records in accordance with current state and regulatory guidelines. + Provides outreach to members via phone to support with care ... ensure standards of practice and policies are in accordance with state and regulatory requirements and provide to providers as needed + Knowledge of existing… more