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Clinical trial associate Jobs in Miami, FL
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Clinical Trial Manager
SABMiami Beach, FL, US- Promoted
- New!
Trial Attorney
CAREERXCHANGE, Inc.Miami, FL, United States- Promoted
Senior Trial Attorney
The Ward Law Group, PLHialeah, FL, US- Promoted
Litigation Trial Partner
CareerxchangeMiami, FL, US- Promoted
Associate Center Clinical Director
ChenMedLudlam, FL, USSr. Trial Attorney
Nationwide Private ClientFlorida, US- Promoted
- New!
Clinical Trial Participants - Earn up to $4k
AFGMiami, FL, United States- Promoted
Commercial Litigation Trial Attorney
JobotMiami, FL, US- Promoted
Construction Litigation Attorney - Trial
Jobot Inc.Miami, FL, US- Promoted
SENIOR ATTORNEY (LEAD TRIAL) - 60065547
State of FloridaMiami, FL, US- Promoted
Trial Attorney
Triumph Professional StaffingCoral Gables, FL, United States- Promoted
Assistant / Associate Professor of Clinical - Anesthesiology
InsideHigherEdCoral Gables, Florida- Promoted
Associate Professor of Clinical - Neurology, Pediatrics
HealthEcareers - ClientMiami, FL- Promoted
Senior Trial Attorney
National LawMiami, FL, United States- Promoted
Trial Attorney Litigation
BCG Attorney SearchMiami, FL, USAssociate Attorney- Appellate / trial support / sophisticated litigation
Solomon Search GroupMiami, FLMCI / MCVI Clinical Research Coordinator 2, Clinical Trial, FT, 8A - 4 : 30P
Miami Cancer Institute at Baptist HealthMiami- Promoted
Clinical Trials - Participate and earn up to $1k+ per trial
carehealth.comHialeah Gardens, FL, United StatesClinical Trial Manager
SABMiami Beach, FL, US- Full-time
Job Description
Job Description
The Clinical Trial Manager (CTM) oversees the planning, implementation and management of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory guidelines. The CTM plays a critical role in coordinating cross functional teams, maintaining budgets, timelines, and quality standards, and ensuring the successful execution of clinical studies.
Duties and Responsibilities (Responsibilities include but are not limited to) :
Study Planning and Execution :
- Lead the design and implementation of clinical trial protocols, including site selection, patient recruitment strategies, and timeline development.
- Contributing to the development of study protocols, protocol amendments, study manuals, Informed Consent Forms (ICFs), Case Report Forms (CRFs), Investigator Brochures (IBs) and other study-related documents as require
- Oversee implementation and maintenance of Trial Master File for inspection readiness
Project Management :
Team Leadership :
Site Management :
Data Integrity and Compliance :
Risk Management :
Communication :
Education / Experience / Skills :
Working Environment and Travel :
Generally accepted office working conditions
Travel up to 25% - ability to travel domestically and internationally
Physical Requirements :
While performing the duties of this job, the employee is regularly required to walk, stand and sit. The employee will be able to use a computer for extended periods at any given time. The employee must regularly lift and / or move up to 10 pounds.
ADA :
The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.
SAB Bio is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. SAB Bio is committed to the principle of equal employment opportunity for all employees and does not discriminate based on race, religion, color, sex, gender identify, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other legally protected status. EOE / AA / Vets
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