Jobs: clinical research

Responsibilities: - Coordinate and oversee clinical research studies from start to finish - Collect and record data accurately and efficiently - Analyze research data and prepare reports for review - Ensure compliance with study protocols, regulations, and ethical guidelines - Collaborate with healthcare professionals, researchers, and study participants -...

About Us">Everest Clinical Research is a leading contract research organization providing comprehensive clinical research services to the pharmaceutical, biotechnology, and medical device industries. We collaborate with renowned companies to advance the development of innovative drugs, biologics, and medical devices.">Job Summary">We are seeking a...

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical...

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical...

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical...

Job SummaryWe are seeking a highly skilled Clinical Research Coordinator/Phlebotomist to join our team at Clinical Research of Ontario. This role will be responsible for coordinating and executing clinical research studies while ensuring the safety and well-being of study participants.Main Responsibilities:Conduct participant assessments and monitor their...

About the RoleWe are seeking a skilled Clinical Safety Data Associate to join our team at Everest Clinical Research. This is an exciting opportunity for a medical professional to contribute to the success of our clinical trials by ensuring the accuracy and quality of safety data.

Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in...

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical...

Job Title**:Clinical Research Coordinator** Company name**:Exdeo Clinical Research Inc.** Pay: $28.00-$35.00 per hour Expected hours: 36 per week Additional pay: - Overtime pay **Benefits**: - Casual dress - Extended health care - Flexible schedule - Work from home Flexible language requirement: - French not required Schedule: - 8 hour shift -...

Overview The Clinical Study Coordinator is responsible for coordinating and executing clinical research studies while ensuring the safety and well-being of study participants. The CRC/CRN bridges clinical care and research, working closely with investigators, participants, and study teams to deliver high-quality, ethical research. Key Responsibilities:1....

Overview The Clinical Study Coordinator is responsible for coordinating and executing clinical research studies while ensuring the safety and well-being of study participants. The CRC/CRN bridges clinical care and research, working closely with investigators, participants, and study teams to deliver high-quality, ethical research. Key Responsibilities:1....

OverviewThe Clinical Study Coordinator is responsible for coordinating and executing clinical research studies while ensuring the safety and well-being of study participants. The CRC/CRN bridges clinical care and research, working closely with investigators, participants, and study teams to deliver high-quality, ethical research.Key Responsibilities:1....

Overview The Clinical Study Coordinator is responsible for coordinating and executing clinical research studies while ensuring the safety and well-being of study participants. The CRC/CRN bridges clinical care and research, working closely with investigators, participants, and study teams to deliver high-quality, ethical research. Key Responsibilities:1....

Clinical Research of Ontario (CRON) is a privately-owned clinical research site dedicated to providing robust services for high-quality, patient-centric clinical studies. CRON focuses on phase I-IV clinical trials across many therapeutic areas. Our Principal Investigators (PI) and Sub Investigators (SI) are board-certified physicians with numerous years of...

Key Accountabilities1. Manage clinical trial programs/projects from one or multiple clients, providing day-to-day technical and operational leadership to project teams supporting these programs/projects.2. Coach, mentor, develop, provide technical review, and provide advice and expertise to direct subordinate Biostatisticians and Statistical Programmers, as...

OverviewThe Clinical Study Coordinator is responsible for coordinating and executing clinical research studies while ensuring the safety and well-being of study participants. The CRC/CRN bridges clinical care and research, working closely with investigators, participants, and study teams to deliver high-quality, ethical research.Key Responsibilities:1....

About the RoleWe are seeking a skilled Clinical Research Associate to join our team as a Safety Data Manager. In this role, you will be responsible for developing study safety data review plans and maintaining a standard set of data review checklists for clinical trial laboratory data, adverse events, and medical events of special interest.You will perform...

verest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices...

Job Summary:We are seeking a skilled Clinical Safety Data Associate to join our team at Everest Clinical Research. The successful candidate will be responsible for developing study safety data review plans and maintaining standard checklists for clinical trial laboratory data, adverse events, and medical events of special interest.About the Role:Develop and...