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Clinical Research Regulatory Manager Jobs

Research Regulatory Specialist Jobs
By Insight Global At New York, NY, United States
-Exceptional communication, analytical, presentation and time management skills
-Excellent working knowledge of regulatory compliance requirements and procedures
-Ability to demonstrate impact on project goals through proactive solutions and keeps management aware of project schedules/timelines.
-Knowledge of MS Office suites, database, spreadsheets, graphic and communications applications
-Extensive knowledge of oncology clinical trials and oncology terminology required.
Clinical Research Compliance Manager
By Weill Cornell Medicine At , New York, 10022, Ny $101,600 - $125,400 a year
Demonstrated organizational skills and ability to pay close attention to detail.
Demonstrated critical thinking and analytical skills.
Demonstrated knowledge of database, word processing, and spreadsheet programs.
Title: Clinical Research Compliance Manager
Approximately five years of prior experience in a clinical research setting.
As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices
Clinical Research Manager Jobs
By Masis Professional Group At United States
Minimum of 5 years' experience working in a Clinical Research Manager or Clinical Project Manager role with relevant experience.
Experience with FDA and US requirements for the conduct of clinical studies is a must.
Multi-disciplinary international project management managing diverse relationships.
Exciting job opportunity with project responsibilities and freedom for professional growths and acquisition of new skills
Supervision (remote and in-person) of participating study centers
Ability to manage multiple projects in parallel and prioritize across study, regulatory, and company goals.
Clinical Research Manager Jobs
By OSF Saint Francis Medical Center At Peoria, IL, United States

Strong leadership abilities to lead an innovative research program.

Clinical Research Project Manager
By Proper Career Solutions At Los Angeles, CA, United States
• MT Group is a CRO for biospecimen sample acquisition and management
1+ years experience in any of the following:
• 2+ years of experience in a science, research, or medical setting
• Full Benefits (Medical, Vision)
As a research coordinator or research associate
• Small, Growing Company (30 people)
Clinical Research Regulatory Manager
By MBO Partners At Charlotte, NC, United States
5-10 years of clinical trial regulatory management experience.
Quality Management System/Regulatory Compliance Program
5 Years minimum regulatory experience in clinical trials
Regulatory certification from AAAHRP, SOCRA, PRIM&R or similar organizations
Experience gained from multiple perspectives: industry sponsor, CRO, academic, government or site level
Has GCP training and follows GCP guidelines and other guidelines related to the conduct of human subject’s research