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 Skill / ability 1 : Ability to lead a research team in the execution of trials within scope of the established study protocol.
Required Skill / ability 2 : Demonstrated skill in meticulous attention to study requirements, regulatory constraints, and accurate follow through.
Ability to prepare and submit regulatory documents and maintenance requirements for the life of the trial(s). Required Skill / ability 3 : Thoroughly skilled in obtaining informed consent and related research subject interactions and requirements.
Proven ability to track multiple occurrences and outcomes and document same in a timely manner. Exceptional organizational skills.
Required Skill / ability 4 : Demonstrated independence and management skills among multiple study sites. Demonstrated ownership of communication requirements necessary for effective oversight and conduct of human clinical research utilizing multiple electronic data capture systems.
Required Skill / ability 5 : Demonstrated ability and skill for laboratory processing and vital sign execution. Preferred Education : Bachelor's degree in health or research related discipline and three years of related work experience in a similar job family.
Experience must indicate ability to work with minimal supervision in a team atmosphere and receptiveness to direction regardless of disease area.
EKG capabilities and phlebotomy skills strongly preferred. Work Week : Standard (M-F equal number of hours per day) Posting Position Title : Clinical Research Nurse 2 University Job Title : YCCI Clinical Research Coordinator Preferred Education, Experience and Skills : Bachelor's degree in health or research related discipline and three years of related work experience in a similar job family.
Experience must indicate ability to work with minimal supervision in a team atmosphere and receptiveness to direction regardless of disease area.
EKG capabilities and phlebotomy skills strongly preferred. Bachelor's of Science Degree in Nursing and four years of related experience or an equivalent combination of education and experience.