Be The Match
Clinical Research Associate I (Trial Monitor) - Remote
This job is now closed
Job Description
- Req#: 2437
Employer Industry: Clinical Research Services
Why Consider this Job Opportunity:
- Competitive salary up to the maximum amount mentioned in the job description
- Opportunity for career advancement and growth within the organization
- Remote work opportunity within the United States
- Supportive and collaborative work environment
- Chance to make a positive impact on clinical research studies
What to Expect (Job Responsibilities):
- Perform site monitoring visits, including source document verification and assessment of site compliance
- Ensure compliance with clinical trial protocols and regulatory guidelines
- Identify and communicate site findings with study personnel and the study team
- Oversee and manage operational aspects of clinical trial sites
- Assist in reviewing study site data to ensure compliance with the study protocol
What is Required (Qualifications):
- Knowledge of clinical research study processes, study design, and protocol management
- Proficiency in computer skills and software applications
- Excellent oral and written communication skills
- Strong time management and problem-solving abilities
- Willingness to travel to sites as necessary
How to Stand Out (Preferred Qualifications):
- Direct experience working at research sites on clinical studies
- ACRP or SOCRA certification
#ClinicalResearch #RemoteWork #CareerOpportunity #CompetitivePay #ProfessionalDevelopment
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We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer.About the company
The Be The Match Registry is the world's largest hematopoietic cell registry, listing more than 22 million individuals and more than 300,000 cord blood units.
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