- Parexel (Raleigh, NC)
- …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant...escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
- Parexel (Raleigh, NC)
- …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant...escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
- Parexel (Raleigh, NC)
- …Study Operations Manager (SOM) + When required Partners with other Study Team members (eg Clinician, Recruitment Specialist, Clinical Data Scientist) + ... + Demonstrated knowledge in disease and technical areas pertaining to clinical studies , including knowledge of company direction, investigational product(s),… more
- Parexel (Raleigh, NC)
- …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant...escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
- Parexel (Raleigh, NC)
- Parexel FSP has an exciting opportunity for a Senior...samples + Provides support for sample related matters to clinical study teams + Works with Informed ... clinical trials. Performs other duties as necessary to ensure optimal clinical trial execution. **Key Accountabilities** **:** ** Study Team Support** +… more
- ThermoFisher Scientific (Greenville, NC)
- …on projects of moderate to high complexity, and may assume regional lead or Clinical Study Manager responsibilities. **Essential Functions** + Manages all ... clinical operational and quality aspects of allocated studies , of moderate to high complexity, in compliance with...requirements, may assume Lead CTM responsibilities on regional level, Clinical Study Manager (CSM) responsibilities… more
- ThermoFisher Scientific (Wilmington, NC)
- …on projects of moderate to high complexity, and may assume regional lead or Clinical Study Manager responsibilities. **Key Responsibilities** : + Manages all ... clinical operational and quality aspects of allocated studies , of moderate to high complexity, in compliance with...requirements, may assume Lead CTM responsibilities on regional level, Clinical Study Manager (CSM) responsibilities… more
- ThermoFisher Scientific (Wilmington, NC)
- **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **CSM ( Clinical Study Manager ):** **OBJECTIVES:** **Lead or ... study operational strategy and planning and oversee execution of select clinical studies (global/regional and/or local country) for assigned clinical … more
- IQVIA (Durham, NC)
- …pre- clinical or Phase I-IV clinical studies . + Consult with Clinical Pharmacology staff on study design, analyses, clinical development plans. + ... **Job Level:** Senior/Principal Pharmacometrician, FSP **Location:** Home-based in the US or Canada...+ Cohesive team environment fostering a collaborative approach to study work. + Variety of therapeutic areas, indications and,… more
- IQVIA (Durham, NC)
- Job Overview Manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained ... of resources to clinical research projects by assigning staff to clinical studies based on their experience and training. * Manage the quality of assigned… more
