Research Coordinator - Clinical Trials Unit

Kennedy Krieger Institute, Inc.; Baltimore (MD); Hybrid; USD 40,000 - 66,000; Full time

Job summary

Kennedy Krieger Institute, Inc. is seeking a Research Coordinator to support clinical trials and studies related to neurological, neurogenetic, neurodevelopmental, and psychiatric conditions.

You will assist with IRB submissions, data management, recruitment, scheduling, and regulatory compliance for diverse age groups. The role requires a Bachelor’s degree in a related field and a minimum of two years of research experience.

Qualifications

• Bachelor’s degree in psychology, neuroscience or related field.
• Minimum two years of research-related work experience.

Responsibilities

• Prepare and submit IRB-required materials and regulatory documentation for local, state, and federal agencies.
• Under the Senior Research Coordinator, assist daily clinical trial and research activities including recruitment and scheduling, study procedures, data collection and documentation.
• Communicate with research collaborators, sponsors, and vendors.
• Manage research data per sponsor and Institute protocols.
• Attend study meetings, conferences, and teleconferences.
• Participate in research planning and development activities.
• Support data preparation, entry, transfer, archiving, maintenance, and analysis; report progress and issues.
• Provide general administrative support including participant reimbursements, inventory, and service billing.
• Collaborate with the Senior Research Coordinator to develop and implement standard operating procedures.

Skills

IRB coordination

Data management

Participant recruitment

Study coordination

Regulatory compliance

Communication

Administrative support

Education

Bachelor’s degree in psychology, neuroscience or related field

Job description

Overview

The Research Coordinator assists and collaborates with the Principal Investigator (PI) and research collaborators for research studies related to neurological, neurogenetic neurodevelopmental and psychiatric conditions in children, adolescents, and adults. This position requires a degree of responsibility, flexibility, and independence to perform diverse duties including collecting, analyzing, and archiving data.

Responsibilities

1. Prepare and submit Institutional Review Board (IRB)-required materials, and prepare compliance and regulatory documentation for local, state, and federal agencies (as well as any other pertinent entity).

2. Under the direction of the Senior Research Coordinator, assist and support daily clinical trial and research study activities, including participant recruitment and scheduling, study procedure scheduling and coordination, obtaining results and ensuring clinician review, and documentation completion.

3. Communicate directly with research collaborators, study sponsors, and study vendors.

4. Manage research data in accordance with protocols established by sponsors and the Institute.

5. Attend study and research related meetings, conferences, and teleconferences.

6. Participate in research planning and development activities.

7. Support data preparation, data entry, transfer, archiving, maintenance, and analysis as needed. Provide and communicate data-related study progress, issues, and problems to research collaborators.

8. Assist with general administrative work, including processing participant reimbursements and incentives, inventory and ordering supplies, and organizing service billing.

9. Work closely with the Senior Research Coordinator to develop and implement standard operating procedures.

Qualifications

EDUCATION:

Bachelor’s degree is required, preferably in psychology, mathematics/statistics, neuroscience, biology, biophysics, physics, chemistry, biochemistry, or another related field.

EXPERIENCE:

Minimum two (2) years of research related work experience required.

Minimum pay range

USD $40,043.12/Yr.

Maximum pay range

USD $66,204.53/Yr.

Job Location : Street 1741 Ashland Ave

# of Hours 40.00

Job Locations US-MD-Baltimore

Pos. Type Regular Full Time

Department : Name Clinical Trials Unit

Equal Opportunity Provider & Employer M/F/Disability/ProtectedVet