PRA Health Sciences
Clinical Research Associate - Home-Based (US)
This job is now closed
Job Description
- Req#: 112085
Employer Industry: Clinical Research
Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Competitive compensation package with comprehensive benefits
- Supportive and collaborative work environment
- Potential for flexible work arrangements, including remote monitoring
- Commitment to continuous learning and professional development
- Inclusive workplace culture that values diversity and equal opportunity
What to Expect (Job Responsibilities):
- Ensure regulatory, ICH-GCP, and protocol compliance while evaluating site performance and providing recommendations
- Conduct Source Document Review and Source Data Verification of site documents and medical records
- Manage reporting of protocol deviations and follow up on identified issues
- Document monitoring activities and maintain accurate communication logs as per SOPs
- Collaborate with site personnel and attend Investigator Meetings to support project objectives
What is Required (Qualifications):
- Bachelor’s degree or RN in a related field or equivalent combination of education, training, and experience
- Minimum of 3 years’ experience as a clinical monitor with experience in virtual and onsite monitoring
- Knowledge of Good Clinical Practice/ICH Guidelines and applicable regulatory requirements
- Excellent communication, presentation, and interpersonal skills
- Ability to manage required travel of up to 75% regularly
How to Stand Out (Preferred Qualifications):
- Demonstrated experience managing complex and high-risk protocols
- Familiarity with systems such as Siebel CTMS, eTMF, and eISF (Florence)
- Proven networking and relationship-building skills
- Strong adaptability to changing technologies and processes
#ClinicalResearch #CareerOpportunity #ProfessionalDevelopment #DiversityAndInclusion #RemoteWork
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