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Clinical Research Specialist
2 months ago
Department Overview:
The George Washington University (GW) Cancer Center, established in 2015, is a collaborative initiative involving the George Washington University, the GW Hospital, and the GW Medical Faculty Associates. Our mission is to enhance GW's commitment to combating cancer through innovative research, education, and equitable healthcare.
Position Summary:
The Clinical Research Coordinator plays a pivotal role in supporting various research initiatives within a designated Practice Area. This role encompasses essential clinical and administrative tasks, including data collection and management, ensuring compliance with regulatory and clinical standards. The Coordinator operates independently to facilitate Investigator-Initiated studies and other research projects across all phases. Responsibilities include conducting clinical trial activities, analyzing research data, and assisting in the preparation of both electronic and paper regulatory submissions, program reports, funding proposals, work plans, activity charts, and correspondence as necessary.
Key Responsibilities:
- Evaluate patient eligibility for studies, gathering necessary medical history and health information as per research protocols. Engage with research participants and their families in a respectful and compassionate manner, ensuring confidentiality.
- Extract clinical data from medical records and charts.
- Execute clinical and administrative tasks required by study protocols, such as measuring blood pressure, performing venipuncture, recording vital signs, completing case forms, and managing regulatory documentation.
- Monitor participant adverse reactions, manage data, and conduct clinical follow-ups. Collaborate with the principal investigator to document and report adverse events.
- Maintain documentation for the institutional review board, including submissions, ongoing reviews, and safety updates.
- Coordinate recruitment efforts for studies, including referrals, advertising, and database research.
- Schedule patient appointments and coordinate necessary testing with relevant departments.
- Prepare study samples for storage and shipping.
- May oversee tracking of study-related income.
- Participate in investigator meetings as required.
- Manage drug maintenance in collaboration with pharmacy services.
- Contribute to the development of new research proposals.
- Perform additional duties as assigned, which may include tasks logically related to the position.
Special Requirements:
Proficient in operating office equipment such as computers, telephones, recorders, calculators, copiers, and pagers. Familiarity with Microsoft Office, OnCore, and other relevant software is essential.
Qualifications:
Applicants should possess a BA/BS degree and a minimum of two years of experience in a related field. The degree must be conferred by the start date of employment. Certification is preferred.
Preferred Qualifications:
- Certifications such as CRCC, CCRA, or CCRP are preferred.
- Strong verbal and written communication skills, along with leadership capabilities.
- Excellent interpersonal, organizational, and problem-solving skills.
- Ability to adapt to changing work duties and responsibilities, with a keen attention to detail.
- Service-oriented mindset with the ability to prioritize tasks effectively.
- Capacity to work collaboratively in a team environment.
- Proficient in managing multiple projects and handling large volumes of information while balancing various priorities.
- Willingness to learn new technical skills pertinent to the role.
- Effective communication with staff, administrators, research scientists, and clinicians.
- Demonstrated proficiency in English and exceptional customer service skills.
Compensation:
The hiring range for this position is $43,000 to $67,889.82.
Benefits:
GW offers a comprehensive benefits package, including medical, dental, vision, life and disability insurance, paid time off, retirement savings, tuition assistance, wellness programs, and various voluntary benefits.
