Essential Duties
- Evaluates and assesses subject's suitability for inclusion in studies; develops and modifies procedures according to study findings; recommends changes to the study protocol to coincide with study goals and objectives. 2. Develops and implements procedures and data quality assurance standards for safety monitoring components of studies. 3. Contributes to designing activities, policies and procedures to improve day to day efficiency of the recruitment and assessment components of the study and to ensure that staff members perform activities within established research protocol. 4. Arranges patient enrollment, determines patient eligibility and obtains informed consent. 5. Develops study subject referral sources; designs and develops outreach programs. 6. Collaborates with multidisciplinary researchers to coordinate research programs that integrate new advances in clinical trials. 7. Delegates tasks and supervises the activities of other licensed and unlicensed care providers. 8. May perform other duties as assigned.
Required Education and Experience
Bachelor's of Science Degree in Nursing and four years of related experience or an equivalent combination of education and experience.
Background Check Requirements
All candidates for employment will be subject to pre-employment background screening for this position, which may include motor vehicle, DOT certification, drug testing and credit checks based on the position description and job requirements. All offers are contingent upon the successful completion of the background check. For additional information on the background check requirements and process visit "Learn about background checks" under the Applicant Support Resources section of Careers on the It's Your Yale website.
Position Focus:
With limited supervision and oversight from the Director of Clinical Research for Neonatology serves as the clinical research coordinator for multiple multi-center and investigator-initiated neonatology related study protocols. Working under the direction of the Director of Clinical Research for Neonatology, plans, tracks and ensures that the clinical activities for study participants are conducted in accordance with approved protocols. These activities include, butare not limited to patient screening, eligibility determination, registration and other protocol and subject milestones. The CRC is also responsible for ensuring timely and accurate data entry into sponsor databases, coordinating monitoring visits conducted by sponsors and other oversight bodies and ensuring timely resolution of sponsor queries. Have clinical experience in a patient-related setting.
Preferred Education, Experience and Skills:
Experience with pediatric phlebotomy.
Posting Disclaimer
The intent of this job description is to provide a representative summary of the essential functions that will be required of the position and should not be construed as a declaration of specific duties and responsibilities of the particular position. Employees will be assigned specific job-related duties through their hiring departments.