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Senior Clinical Research Associate
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Job Description
- Req#: D0326AF1D5
Employer Industry: Clinical Research Organization (CRO)
Why consider this job opportunity:
- Salary up to $145,000 per year
- Comprehensive benefits package including medical, vision, dental, HSA, FSA, life and disability insurance, and 401(k)
- Opportunity for career advancement and growth within a stable and thriving company
- Flexibility to work remotely and maintain a healthy work-life balance
- Collaborative culture that values diversity, inclusion, and employee well-being
What to Expect (Job Responsibilities):
- Perform all site monitoring visit activities, including all study visit types (PSV, SIV, IMV, and COV)
- Participate in the site selection process with oversight from the Clinical Team Lead
- Provide feedback to assist sites with resolution of deficiencies and follow-up until resolved
- Contribute to the development and review of protocols, study tools, and documentation for clinical trials
- Mentor, train, and co-monitor junior clinical team members
What is Required (Qualifications):
- BA/BS, preferably in a life science, nursing, pharmacy, or related field
- Approximately 4-5 years of on-site monitoring experience within the CRO, pharmaceutical, or biotechnology industry
- Proficiency in MS Office and use of EDC systems
- Strong written, verbal, and presentation skills
- Commitment to quality and attention to detail in managing multiple sites and protocols
How to Stand Out (Preferred Qualifications):
- Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
- High-character individual with a collaborative spirit and willingness to learn
- Critical thinking skills with the ability to craft novel solutions
- Experience in business development meetings or the RFP process
- Ability to adapt quickly to changing environments and embrace risks
#ClinicalResearch #CRO #CareerOpportunity #CompetitivePay #DiversityAndInclusion
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