Job Description

Position Purpose
To support The Department of Epidemiology at Geisel School of Medicine at Dartmouth in achieving its mission to conduct rigorously constructed research and apply state-of-the-art and novel methods and technologies to advance the field of epidemiology and impact human health and disease. In collaboration with project leaders, the Research Project Coordinator will coordinate the implementation and ongoing activities for a large National Institute of Health (NIH) funded Environmental influences on Children’s Health Outcome (ECHO) birth cohort study.
Description
Required Qualifications - Education and Yrs Exp Bachelors plus 6 or more years' experience or combination of education and experience
Required Qualifications - Skills, Knowledge and Abilities
• Bachelor’s degree in health or social sciences, or the equivalent combination of education and experience is required.
• One to two years’ experience as a study coordinator in a comparable setting.
• One to two years’ experience recruiting and interviewing research participants or other comparable experience.
• Demonstrated ability to coordinate a complex research project with minimal supervision.
• Demonstrates a high degree of independence and responsibility for ensuring timely completion of project activities.
• Proficiency with Microsoft Suite and web-based applications.
• Ability to apply critical thinking and sound judgment to address open-ended problems.
• Superior verbal communication and writing skills.
• Proven ability to manage multiple competing priorities.
• Must complete educational requirements for Dartmouth Committee on the Protection of Human Subjects (IRB) upon hire and appropriate laboratory and safety training(s).
• Must have a valid driver’s license and be willing to travel to other study sites in the region of the research study as needed.
Preferred Qualifications
• Master’s degree in health or social sciences or the equivalent combination of education and experience.
· One to two years’ experience in a medical or clinical environment with direct patient contact
Description
Recruitment, Interviewing and Measurement/ Specimen Collection
· Responsible for recruitment/enrollment of study participants remotely and/or in person.
· Coordinates, schedules, and completes recruitment activities using established study protocols.
· Implements the research activities including distribution and completion of surveys, data collection and management, subject identification, recruitment, interviewing, and scheduling.
· Maintains a high level of research professionalism to maintain participant engagement and retention.
· Provides education and instruction to participants on informed consent, study materials, collection of samples, measurements, and follow-up processes according to protocols.
· Conducts necessary follow-up activities as needed and coordinates with laboratory and other study personnel to ensure specimens and measurements are collected, processed, entered into databases, and delivered according to protocol.
· Enters accurate study data in established databases in a timely manner according to protocols.
Percentage Of Time 50%
Description
Coordination
· Works closely with the principal investigator and research directors on the development of, revisions and updates to protocols, study materials, and supplies.
· Maintains close communication with the principal investigator, study research directors, and other study staff regarding study progress, processes, and the collection and delivery of samples.
· Assists study research directors with data monitoring and tracking activities, preparation of reports, Institutional Review Board (IRB) renewals and revisions, and coordination of other administrative activities as needed.
· Coordinates collection and delivery of samples with laboratory, clinics, hospital staff, and other study staff as needed.
· Maintains study supplies, equipment, and materials.
Percentage Of Time 20%
Description
Medical Records
· May conduct medical record reviews according to study protocols and may act as a clinical resource to other study staff for medical record reviews.
· Maintains working relationships with medical and administrative staff to coordinate medical record review activities.
Percentage Of Time 5%
Description
Data Management
· Ensures that data are successfully collected and managed.
· Ensures that subject and data confidentiality is maintained, and data integrity is maintained.
· Generates pertinent reports on a monthly or as-needed basis. Assists in the organization of study-related protocols on the server.
Percentage Of Time 10%
Description
Project Support
· Coordinates periodic review and update of protocols and assists in preparation of materials for IRB requests and renewals.
· Maintains accurate and efficient tracking system for study documents approved by IRB and assures protocol materials are up to date and distributed appropriately.
· Coordinates mailings for study subjects, follows up with staff on missing forms and materials, and maintains a supply of materials for staff.
Percentage Of Time 10%
Description
Miscellaneous
· Other study tasks as needed
· Adheres to the most current public health recommendations regarding COVID-19, including symptom surveillance, screening questions, and personal protective equipment.