Senior Research Coordinator - Clinical Trials Unit

Socket.dev; Baltimore (MD); On-site; USD 51,000 - 88,000; Full time

Job summary

Socket.dev in the United States is seeking a Senior Research Coordinator for the Clinical Trials Unit to manage complex multi-study projects in pediatric psychiatry.

You will oversee IRB submissions, protocol adherence, data management, and specimen handling in DOT/IATA compliant shipments, while coordinating patient visits and study procedures.

This role requires a Bachelor's degree and at least four years of research experience; a Master's is preferred.

Qualifications

• Bachelor’s degree in psychology, statistics, or neurosciences.
• Requires at least four (4) years of research-related work experience.
• Master’s degree preferred.

Responsibilities

• Prepare and submit IRB materials and regulatory documents.
• Manage IRB activities: initial applications, amendments, annual reviews, terminations.
• Ensure protocol adherence across multiple studies and educate staff on compliance.
• Develop site-specific study documentation and routine reports.
• Coordinate participant recruitment, scheduling, visits, and study procedures.
• Collect and ship specimens per DOT/IATA regulations.
• Lead data management, entry, transfer, archiving, and analysis tasks.
• Attend study meetings and contribute to SOP development.

Skills

Project management

IRB processes

Regulatory compliance

Data management

Clinical trials

Communication

Education

Bachelor's degree

Master's degree

Job description

Overview

The Senior Research Coordinator in the Clinical Trials Unit will be primarily responsible for complex project management for multiple research studies related to psychiatric conditions in pediatric patients. Activities include but are not limited to project execution, implementation, daily administration and close out for multiple research studies. The Senior Research Coordinator will ensure precise implementation of and adherence to study protocol, create all study documentation, oversee operating procedures, timelines, IRB applications, data preparation, and other research-related activities. In addition to operational management of multiple research studies, the Senior Research Coordinator will see patients participating in ongoing clinical trials, and will be responsible for specimen collection, processing, and DOT/ IATA compliant handling and shipment.

Responsibilities

1. Prepare and submit Institutional Review Board (IRB) required materials, as well as prepare compliance and regulatory documentation for local, state, and federal agencies and any other pertinent entity.
   1. Manage ongoing IRB activities including preparation and submission of initial applications, changes in research, protocol deviations, annual continuing reviews, and termination reports.
   2. Create and maintain multiple IRB accounts and investigator notebooks and report adverse events.
2. Implement and ensure adherence to protocol for multiple studies simultaneously.
   1. Respond to questions regarding protocol content from site staff.
   2. Continuously educate and train personnel, patients, and caregivers on protocol compliance.
   3. Identify protocol problems, inform investigators, and assist in problem resolution efforts.
3. Develop protocol compliant site-specific study documentation for multiple studies. Responsible for developing and producing custom and routine reports as necessary.
4. Conduct ongoing clinical trial and research study activities with minimal direction. Such activities include:
   1. (1) participant recruitment and scheduling,
   2. (2) study procedure scheduling and coordination,
   3. (3) conducting patient visits and executing study procedures,
   4. (4) managing specimen collection and processing,
   5. (5) obtaining results and ensuring clinician review,
   6. (6) documentation completion, and
   7. (7) reporting.
5. Administer blood draws via venipuncture, ECGs, and collect vital signs for pediatric patients. Process and ship collected biomaterials in accordance with DOT and IATA hazmat regulations.
6. Responsible for independent project management of multiple research studies and regular communication with research collaborators, study sponsor, and study vendors.
7. Manage research data in accordance with protocols established by sponsors and the Institute. Lead efforts on data preparation, data entry, transfer, archiving, maintenance, and analysis as needed. Provide and communicate data-related study matters to research collaborators.
   1. Oversee deliverables for monitoring requirements, site initiation visits, review and approval of monitoring plan; ensure monitoring is conducted in accordance with Standard Operating Procedures (SOPs) and monitoring plan; ensure timeliness of monitoring and follow-up action items are completed.
   2. Responsible for resolving all study-related queries, final study closeout, and lock of databases.
8. Attend study and research-related meetings, conferences, and teleconferences.
9. Develop and maintain SOPs, for the program and the Institute, that adhere to and promote to the tenets of Good Clinical Practice.
10. Participate in research planning, development, and legacy activities.
11. Assist with general administrative work, including: processing subject reimbursements and incentives, inventory and ordering supplies, and organizing service billing.

Qualifications

EDUCATION:

• Bachelor’s degree is required, preferably in psychology, statistics, or neurosciences.
• Master’s degree preferred.

EXPERIENCE:Requires at least four (4) years of research related work experience.

Minimum pay range

USD $50,786.11/Yr.

Maximum pay range

USD $87,503.31/Yr.