Study Coordinator - High Point, NC
About The Position
The Central Study Coordinator position is responsible for the coordination and support of remote site activities for assigned projects and must reside in or near High Point, NC. For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
Requirements
- Ability to manage technology and web-based research platforms on PC (Microsoft OS) laptop in the remote workspace.
- Study Tearn experience is ideal.
- Critical thinking skills.
- Strong communication Skills (verbal and written).
- Ability to work independently, and collaboratively with other CSCs to delegate tasks as needed.
- Working location that has the ability to maintain privacy.
- Current knowledge of and the ability to apply ICH / GCP and applicable regulations and guidelines.
- Competent in the application of standard business procedures including but not limited to SOPs, global regulations.
- Well organized and able to multitask.
- Able to work independently and as a team member.
- Able to take initiative while following directives.
Responsibilities
- Serve as point of contact for day-to-day Site communications, document submissions and activity coordination.
- Support pre-screening, screening and recruitment activities, as assigned.
- Responsible for subject re-consenting, acquiring medical records, conducting protocol activities, as directed by the Principal Investigator.
- Perform data-entry, evaluate and respond to system queries and monitor clinical databases as assigned.
- Establish and maintain timely Site communication as assigned.
- Maintain documentation which complies with IRB/FDA policies.
- Assist with study closeout.
- Assist site with other study-related activities as directed.
- Other duties as assigned.
Benefits
- Diversity, equity, and inclusion initiatives
- Encouragement of innovative, collaborative, and entrepreneurial spirits
- Safe space where all employees feel empowered to succeed
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
