- Parexel (Raleigh, NC)
- **Job Summary** The Patient Compensation Lead in Clinical Development & Operations will be responsible for ensuring all processes and vendors are in place to enable ... services, including sourcing, technology, and defining roles and responsibilities + Lead cross-functional efforts to identify and implement improvements to payments… more
- Parexel (Raleigh, NC)
- …tasks and time per task contracted) and according to the assigned role (Global Lead Physician GLP or Regional Lead Physician RLP). Medical support includes but ... leaders, solution consultants + Participate in team project and investigator meetings + Provide training of study teams on...a Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability to… more
- Parexel (Raleigh, NC)
- …support of company products and projects. This individual will work with the lead and/or program medical writer and independently to develop messages and write, ... documents for clarity, and accuracy according to Sponsor standards. - Work with lead writer and project team to develop document messages and data presentations… more
- Parexel (Raleigh, NC)
- …and time per task contracted) and according to the assigned role (Global Lead Physician or Regional Lead Physician). **Medical Expertise** and experience in ... + Experience as a Physician in Industry or as a clinical trial investigator is required + Previous CRO experience is strongly preferred + Medically qualified… more
- Parexel (Raleigh, NC)
- …support of company products and projects. This individual will work with the lead and/or program medical writer and independently to develop messages and write, ... documents for clarity, and accuracy according to client standards.. + Work with lead writer and project team to develop document messages and data presentations… more
- GRAIL (Durham, NC)
- …cross-functionally to proactively manage both GCP and CDx regulatory risks, lead inspection readiness, and continuously improve quality standards utilizing insights ... from inspections, audits, and evolving regulatory landscapes. **Responsibilities:** + Lead and manage internal processes and systems, clinical and diagnostic quality… more
- Pfizer (Sanford, NC)
- …We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include ... a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental… more
- Parexel (Raleigh, NC)
- …making changes to contract templates within the Legal division approved parameters + Lead study level site contracting activities, direct other ICL and act as ... tasks of moderate scope and complexity in applicable discipline **Collaboration** + Lead and develop relationships with key investigational sites and Site Management… more
- Elevance Health (Durham, NC)
- **Clinical Fraud Investigator II - Registered Nurse and CPC - Calrelon Payment Integrity SIU** **Location:** This role requires associates to be in-office 1 - 2 days ... eliminate and prevent unnecessary medical-expense spending. The **Clinical Fraud Investigator II** is responsible for identifying issues and/or entities that… more
- Rubrik (Raleigh, NC)
- …to operate effectively within a highly regulated environment. **What you'll do:** + Lead and act as the primary investigator during incident response (IR) ... needed to protect the organization. As the Security Operations Incident Response Team Lead , FedRAMP you will be responsible for leading and mentoring a team of… more
- Chiesi (Cary, NC)
- …the Core Team, ensuring the clinical perspective informs key strategic decisions. + Lead the Clinical Team in designing and executing a comprehensive global clinical ... in the pharmaceutical/biotech industry, or 7-10 yrs in academia with clinical investigator track record. + Experience within the specific therapeutic area is… more
- United Therapeutics (Research Triangle Park, NC)
- …clinical trials and registries and other real-world evidence generation. Individual will lead development of the statistical analysis plan, ensure data integrity and ... for publication into abstracts, posters and manuscripts. + Act as the lead project statistician for assigned phase 3b/4 clinical trials, leading the development… more
- Sumitomo Pharma (Raleigh, NC)
- …development plan(s) for assigned asset(s) and serve as the Clinical Research Lead for stem cell program within the Ophthalmology therapeutic area. **Job Duties ... and Responsibilities** + Responsible for and lead all activities related to clinical study design from...clinical study reports + Contributes to the preparation of Investigator Brochures, annual reports, data collection systems and final… more
- Sumitomo Pharma (Raleigh, NC)
- …and mentoring. **Job Duties and Responsibilities** + As a Regional Regulatory Lead , manage regional (United States, European and/or ROW) regulatory activities as ... with the global registration strategy of the product + Supports the global regulatory lead (GRL) and the CMC regulatory lead in the formulation of regulatory… more
- Eaton Corporation (Raleigh, NC)
- …business considerations. The Chief Engineer - Aerospace Electrification will initiate, lead , and create research and develop emerging technology programs for ... applications within the Energy Systems team. You will be a principal investigator on key projects responsible for developing and meeting project schedules, defining… more
- Sumitomo Pharma (Raleigh, NC)
- …Regulatory Leader (GRL) for assigned projects. This position is expected to lead the development and implementation of regulatory strategy from proof of concept, ... staff Phases I-IV Research & Development Activities + As a Regional Regulatory Lead , manage regional (United States and/or European) regulatory activities as part of… more
- United Therapeutics (Research Triangle Park, NC)
- …and writing, including clinical study reports, clinical study protocols, and investigator 's brochures. You also bring strong experience in external-facing scientific ... documents including but not limited to: clinical study protocols and reports, Investigator 's Brochures, and safety documents that may be submitted to the Food… more
- Merck (Raleigh, NC)
- …and goals for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies. The RMSD serves as a role model for ... Enhances the comprehension of the scientific foundations and goals of investigator -sponsored research + Identifies barriers to patient enrollment and retention… more
- IQVIA (Durham, NC)
- …translating into appropriate budgets/contract exhibits for company sponsored and investigator initiated clinical trial agreements and other ancillary contract ... documents as they relate to various clinical projects.Analyze investigator grants for fair market value aligned with regional knowledge and the J&J pricing… more
- IQVIA (Durham, NC)
- …Associate Clinical Project Management Director/Trial Delivery Manager (TDM) to lead and coordinate global and regional clinical trial management activities. ... delivery of trial milestones. **Key Responsibilities:** **Trial Oversight & Management** + Lead the Study Management Team and provide regular updates on trial… more
