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Clinical Research Associate II

Mass General Brigham

Boston (MA)

Remote

USD 65,000 - 85,000

Full time

Yesterday
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Job summary

Mass General Brigham offers an opportunity in clinical research, focusing on tracking clinical trials across various sites. This role includes responsibilities like conducting monitoring visits and ensuring compliance with study protocols. Candidates should possess a bachelor's degree and have experience in clinical research, alongside strong organizational and communication skills. The job supports remote work, encouraging candidates to grow in a collaborative environment.

Benefits

Opportunity for career advancement and growth
Supportive and collaborative work environment
Competitive salary

Qualifications

  • Minimum of 1-2 years of directly related work experience in clinical research.
  • Strong written and verbal communication skills.
  • Ability and willingness to travel nationally for monitoring visits.

Responsibilities

  • Track the progress of clinical trials across participating sites.
  • Conduct onsite and remote monitoring visits, completing necessary reports.
  • Verify documentation and compliance with study protocols.

Skills

Organizational skills
Time management
Communication
Problem-solving
Analytical abilities

Education

Bachelor’s degree

Job description

Employer Industry: Healthcare and Clinical Research

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Work remotely from anywhere in the U.S. (with some travel required)
- Supportive and collaborative work environment
- Engage in meaningful work that contributes to groundbreaking medical research
- Competitive salary with a structured work schedule (40 hours per week)

What to Expect (Job Responsibilities):
- Track the progress of clinical trials across participating sites, including accrual and regulatory submissions
- Correspond with sites to address questions and provide updates on trial activities
- Conduct onsite and remote monitoring visits, completing necessary reports
- Verify documentation and compliance with study protocols to ensure participant eligibility
- Gather and organize essential regulatory documents from participating sites

What is Required (Qualifications):
- Bachelor’s degree required
- Minimum of 1-2 years of directly related work experience in clinical research
- Exceptional organizational and time management skills with attention to detail
- Strong written and verbal communication skills
- Ability and willingness to travel nationally for monitoring visits

How to Stand Out (Preferred Qualifications):
- Working knowledge of clinical research protocols
- Ability to work independently with minimal supervision
- Demonstrated problem-solving skills and analytical abilities
- Experience with remote work environments

#ClinicalResearch #HealthcareCareers #RemoteWork #CareerGrowth #OncologyTrials

We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately. 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.

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