- IQVIA (Durham, NC)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director/Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures the successful planning, execution, and closure of clinical trials, whether… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …and services in more than 110 countries and regions. Provides leadership and project management support essential to the successful development of strategic new ... + Typically requires 12 years of pharmaceutical environment experience that includes project management and leading several multi-functional teams + Excellent… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …and services in more than 110 countries and regions. The Clinical Research Associate assists in the management of the clinical monitoring process to ... IVRS set-up, central lab set-up, and other vendor selection processes. + Maintaining clinical trial management system (CTMS) information pertaining to the study… more
- Catalent Pharma Solutions (Greenville, NC)
- ** Associate Project Manager** **Position Summary** Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in ... safety of every patient, consumer and Catalent employee. The Associate Project Manager partners with the site... Project Manager partners with the site project management team to facilitate inventory tracking,… more
- IQVIA (Durham, NC)
- IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in GLP-1/Obesity/Diabetes (Type II) or Cardiovascular clinical trials. ... drive, and track subject recruitment plan in line with project needs to enhance predictability. * Administer protocol and...* If applicable, may be accountable for site financial management according to executed clinical trial agreement… more
- Parexel (Raleigh, NC)
- …Clinical Research Associate (Sr. CRA) is responsible for the site management , site monitoring and close-out of assigned clinical trials investigator sites ... documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management , study progress and metrics + Identify… more
- Sumitomo Pharma (Raleigh, NC)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The ... associate medical director is responsible for the leadership, development, and management of clinical studies while building and maintaining relationships… more
- Parexel (Raleigh, NC)
- …Clinical Research Associate (Sr. CRA) is responsible for the site management , site monitoring and close-out of assigned clinical trials investigator sites ... documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management , study progress and metrics + Identify… more
- Parexel (Raleigh, NC)
- …with late-phase clinical research. + Understanding of RWD platforms, project management systems, and GCP environments. **Education:** Bachelor's degree in ... for innovative RWD projects. We're looking for a **strategic project leader** with strong communication skills, adaptability, and a...a science or clinical -related field; Prince II or AMPM certification preferred. **Why… more
- Parexel (Raleigh, NC)
- …we are expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global Immunology and Inflammation ... Therapeutic Franchise. As an Associate / Medical Director, you will work closely with...with feasibility leaders, solution consultants + Participate in team project and investigator meetings + Provide training of study… more
- IQVIA (Durham, NC)
- ** Associate Director, Client Services - Clinical Trial Payments** **Overview** IQVIA is a leading global provider of advanced analytics, technology solutions, ... and clinical research services to the life sciences industry. IQVIA...required. + This role requires 5+ years of relevant project , client, and people management experience. +… more
- WCG Clinical (Cary, NC)
- …as the business subject matter expert between DAI Solutions and Product Management , translating business, clinical , and user requirements into actionable product ... Data Analytics & Insights (DAI) Product Solutions, Associate Director (Remote) **General Information** **Location:** Cary, NC,...21CFR Part 11, GCP, GDPR) and best practices in clinical data management /analytics. + Proficiency in MS… more
- ThermoFisher Scientific (Greenville, NC)
- … and oversight of all contracted services. **Discover Impactful Work:** The Associate /Medical Director provides medical oversight of clinical trials to ensure ... Understanding guidelines (FDA, ICH, EMA and GCP) + Working knowledge of biostatistics, data management , and clinical operations procedures + Ability to act as a… more
- Sumitomo Pharma (Raleigh, NC)
- …a dynamic, highly motivated, and experienced individual for the position of ** Associate Director, Regulatory Affairs (Oncology).** The Associate Director is part ... (HA) information requests. In addition, this position may represent GRA in project related meetings, develop regulatory strategy and provide regulatory input as… more
- ThermoFisher Scientific (Wilmington, NC)
- …/oversight, including significant study management support experience (eg clinical trial assistant/ associate or lead CRA). Experience could include ... local country requirements is also required.** **Demonstrated successful experience in project /program management and matrix leadership** **E.g. timeline/budget … more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- …with study team and key stakeholders across different functional areas such as clinical , regulatory affairs, asset management , safety and clinical operation. ... needs and nutraceutical products for the maintenance of everyday health. As an Associate Director, Biostatistician, you will be a champion of Otsuka's culture and… more
- United Therapeutics (Raleigh, NC)
- …with teammates and appreciate the opportunity to collaborate with senior management , CPLs, MSL Field Directors, MSLs, Medical Communications and Medical Information, ... in onboarding for non-GMA new hires in need of clinical training + Execute training programs using knowledge of...to ensure training strategy remains relevant. Based on overall project strategy and priorities, propose, plan, and develop new… more
- Catalent Pharma Solutions (Greenville, NC)
- …Candidate** + Bachelor's degree in science with at least five years of pharmaceutical project management experience (preferably in the CDMO industry); or; + ... Associate degree in science with at least six years of pharmaceutical project management experience (preferably in the CDMO industry) or; + High school… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …medicines, solutions and services in more than 110 countries and regions. Quality Associate II / Quality Associate III, QA QA FC Release Certifications ... other supplemental documents to support these submissions. **Summary:** The Quality Associate II/II provides routine technical support for various tasks (ie… more
- Parexel (Raleigh, NC)
- …English required + Proficient in local language, as applicable, preferred + Project management and organizational skills + Ability to effectively multi-task ... Parexel FSP has an exciting opportunity for a Senior Precision Medicine Associate . This role works closely with line Manager, Precision Medicine, and other key… more