PRA Health Sciences
Clinical Research Associate - Home-Based (US)
This job is now closed
Job Description
- Req#: 111399
Employer Industry: Clinical Research Organization
Why Consider this Job Opportunity:
- Competitive total reward package including variable pay and recognition programs
- Best in class employee benefits and supportive policies
- Opportunities for career development and continuous learning culture
- Ability to work with engaging projects that enhance professional development
- Inclusive and equal opportunity employer fostering a discrimination-free workplace
What to Expect (Job Responsibilities):
- Ensure regulatory, ICH-GCP, and protocol compliance
- Conduct monitoring activities using various methods, including on-site and remote
- Manage reporting of protocol deviations and ensure timely query resolution
- Document activities via follow-up letters, monitoring reports, and other project documents
- Review data entry timeliness, site signature sheet, and delegation of duties log
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 virtual and onsite monitoring experience
- Proficiency in Good Clinical Practice/ICH Guidelines and other regulatory requirements
- Excellent communication, presentation, and interpersonal skills
- Ability to travel up to 75% on a regular basis
How to Stand Out (Preferred Qualifications):
- Knowledge of systems like Siebel CTMS, eTMF, eISF (Florence)
- Demonstrated experience in managing complex and high-risk protocols
#ClinicalResearch #CareerDevelopment #RegulatoryCompliance #ProfessionalDevelopment #InclusiveWorkplace
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