Benefits:

401(k)

Dental insurance

Health insurance

Vision insurance

We are seeking an energetic Clinical Research Coordinator (CRC) to join our team.

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The CRC is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring a high level of knowledge of study specific protocols, as well as coordination and collaboration with research colleagues and departments.

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Duties and Responsibilities

Perform study procedures in accordance with GCP and study protocols

Coordinate protocol related research procedures, study visits, and follow-up care

Organize and maintain paper and electronic study data in a complete and correct manner

Work closely with recruitment and pre-screening teams to meet study enrollment goals

Adhere to an IRB approved protocol

Participate in the informed consent process of study subjects

Support the safety of clinical research patients/research participants

Maintain study source documents

Report adverse events

Educate subjects and family on the protocol, study intervention, study drug, etc.

Comply with Institutional policies, standard operating procedures (SOPs) and guidelines

Complete case report forms (paper & electronic data capture) and address queries

Facilitate study initiation, monitoring visits, and close out activities

Retain records/archive documents after study close out

Requires effective writing and communication, work as part of a team, ability to multitask

Act as liaison for research subject, investigator, IRB, sponsor, and healthcare professionals

Document investigational product (drug/device) accountability

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Qualifications

Bachelor’s Degree required; degree in Biology and/or Psychology field preferred

Must be willing and able to work in a clinical setting involving a psychiatric/mentally disabled population

Must have ability to read and understand clinical trial protocols

Must have attention to detail and the ability to handle multiple tasks with precision

Must be adept with computers

Must possess excellent critical thinking skills

Must have excellent interpersonal and communication skills and be a hardworking team player

Must possess strong data management skills

Familiarity with medical terminology/environment required

Available for full-time onsite position (40 hrs/week)