Clinical Research Specialist
About The Position
As a Research Specialist, you will lead and manage complex clinical research, collaborating with Principal Investigators to ensure protocol adherence and scientific integrity. You will actively contribute to study design and methodology to advance research objectives. Every day you will oversee data collection, management, and quality control, ensuring accuracy and regulatory compliance. You will analyze data, prepare detailed reports, and contribute to presentations and publications. To be successful in this role, you will possess advanced knowledge of research methodologies and regulatory guidelines, demonstrating exceptional problem-solving and critical thinking skills. Your ability to manage multiple projects, mentor junior staff, and communicate complex scientific information effectively is essential. Coordinates and schedules subject study visits to ensure adequate supplies, procedures and investigator availability. Provides study specific, individualized education to study subjects and families. Ensures all appropriate subject consents are obtained. Collects and processes protocol required specimens. Acts as a liaison between Sponsor, Investigator, and Study Subject Collects all required study data and completes CRFs in a timely, accurate manner.
Requirements
- Associates Other in related field or an equivalent combination of relevant education and job-related experience in lieu of a degree, upon hire
- Minimum 2 years related experience
Nice To Haves
- Advanced knowledge of research methodologies and regulatory guidelines
- Exceptional problem-solving and critical thinking skills
- Ability to manage multiple projects
- Ability to mentor junior staff
- Ability to communicate complex scientific information effectively
- Bachelors Other in related field
- 3+ years clinical experience, upon hire
Responsibilities
- Lead and manage complex clinical research, collaborating with Principal Investigators to ensure protocol adherence and scientific integrity.
- Contribute to study design and methodology to advance research objectives.
- Oversee data collection, management, and quality control, ensuring accuracy and regulatory compliance.
- Analyze data, prepare detailed reports, and contribute to presentations and publications.
- Coordinate and schedule subject study visits to ensure adequate supplies, procedures and investigator availability.
- Provide study specific, individualized education to study subjects and families.
- Ensure all appropriate subject consents are obtained.
- Collect and process protocol required specimens.
- Act as a liaison between Sponsor, Investigator, and Study Subject.
- Collect all required study data and complete CRFs in a timely, accurate manner.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
Number of Employees
5,001-10,000 employees
