- 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 (Chicago, IL)
- …Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed ... guidelines from different sponsors and/or monitoring environments (ie FSO, FSP , Government, etc.). Acts as a site processes specialist,...study conventions (eg Clinical Trial Management System, CTMS). Performs QC check of… more
- Parexel (Richmond, VA)
- …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 (Columbus, OH)
- …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 (Austin, TX)
- …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
- ThermoFisher Scientific (West Hills, CA)
- …Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed ... through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development...study conventions (eg Clinical Trial Management System, CTMS). Performs QC check of… more
- ThermoFisher Scientific (Carlsbad, CA)
- …Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed ... study conventions (eg Clinical Trial Management System). + Facilitates effective communication between investigative sites, the client company and the PPD project… more
- ThermoFisher Scientific (Austin, TX)
- …Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed ... study conventions (eg Clinical Trial Management System). Facilitates effective communication between investigative sites, the client company and the PPD project… more
- ThermoFisher Scientific (Chicago, IL)
- …Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed ... study conventions (eg Clinical Trial Management System). Facilitates effective communication between investigative sites, the client company and the PPD project… 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 (Austin, TX)
- …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 (Jefferson City, MO)
- …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
- BeOne Medicines (San Mateo, CA)
- …_Line management responsibilities:_ + Provides leadership, management, and/or mentorship to clinical study managers at various levels for assigned portfolio ... as required with external, global and/or regional stakeholders such as eg, FSP partners, clinical operations leaders in other regions, and monitoring… more
- BeOne Medicines (Emeryville, CA)
- …responsibilities:_ + Provides leadership, management, and/or mentorship to associate directors, clinical study managers at various levels for assigned portfolio ... as required with external, global and/or regional stakeholders such as eg, FSP partners, clinical operations leaders in other regions, and monitoring… more
- IQVIA (San Diego, CA)
- …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 (Suwanee, GA)
- …Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed ... clinical research services provide end-to-end support for clinical trials from study start up to...clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies . Our Clinical Operations… more