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Project Management Specialist, Optimized Trials
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Job Description
- Req#: 3702243
Employer Industry: Clinical Research
Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Supportive and collaborative work environment
- Chance to make a positive impact on clinical trial outcomes
- Engaging role that combines organizational, technical, and communication skills
- Work with cross-functional teams to achieve business results
- Involvement in the management of significant healthcare projects
What to Expect (Job Responsibilities):
- Set up, maintain, and close out project files and study information, including regulatory documents and enrollment data
- Track milestone progress in real-time and assist with contingency plans for delays
- Prepare regulatory documents for IRB/IBC approvals and coordinate research monitoring activities
- Record the status of milestones and key performance indicators, providing updates to the Project Manager
- Facilitate the collection and management of medical records as per the scope of clinical trials
What is Required (Qualifications):
- Minimum educational requirement: BS/BA in Life Science or related discipline
- At least one (1) year of clinical research experience or experience in a healthcare setting
- Strong interpersonal skills and ability to build positive relationships
- Excellent verbal and written communication skills
- Thorough understanding of HIPAA privacy and security laws around PHI
How to Stand Out (Preferred Qualifications):
- Previous GCP training and certification
- Experience working with electronic medical records (EMRs)
- Proficiency with Clinical Trial Management Systems (CTMS) and Electronic Document Management Systems (EDMS)
- Data entry experience
#ClinicalResearch #Healthcare #CareerOpportunity #ProjectManagement #RegulatoryCompliance
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