- 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
- 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)
- …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
- 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
- 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
- ThermoFisher Scientific (Wilmington, NC)
- …and mentoring to your staff regarding all general aspects of the Clinical Team Manager (CTM) and Clinical Manager roles. You will be responsible for ... within an area of a region to secure the successful completion of clinical deliverables within assigned studies . This includes training and managing staff… 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
- Parexel (Raleigh, NC)
- …investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical ... /scientific writing skills. + Scientific background essential; writing experience includes multiple clinical documents: study reports, study protocols, or… more
- Parexel (Raleigh, NC)
- …Senior Medical Writer will research, create, and edit all documents associated with clinical research. The Senior Medical Writer may operate as the project lead ... providing client liaison and proposals input. **Key Accountabilities** : **Author Clinical Documents** + Gather, review, analyze, and evaluate pertinent resources to… more
- IQVIA (Durham, NC)
- …multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models.** **Apply now ... You'll Do** + Lead data management for complex, global clinical trials from study setup to database...+ Your previous roles/job titles may include _Clinical Data Manager , Senior Clinical Data Manager ,… more
- ThermoFisher Scientific (Wilmington, NC)
- …and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies . The PPD FSP Solution: PPD's Functional Service ... set programs up for success. Joining within our PPD FSP functional area, allows you to join the renowned... studies from Final Protocol Concept Sheet to Clinical Study Report (CSR) and applicable results… more