Clinical Research Coordinator II; Part time

We are hiring Clinical Research Coordinator II (Part time).

Please let me know if you are interested or anyone who might be interested.

Client:
Major Clinical Research Client

Position:
Clinical Research Coordinator II (Part time)

Duration: 12+ Months Contract

Pay Rate: $26.00-$29.00/ Hr on W2

Work Schedule:

20 hours per week (
Must be a Nurse
)

• Manages multiple ongoing clinical trials involving patients or healthy volunteers.
• Completes all required documentation to capture study data as outlined in the protocol, while ensuring participant safety, understanding, and cooperation throughout the study.
• Works closely with the research site team and cross-functional staff.
• Supports overall site operations, including recruitment, enrollment, and retention of study participants.

• Conducts clinical studies in compliance with FDA, GCP, and ICH regulations and guidelines.
• Provides medical care to participants, prioritizing patient safety at all times.
• Schedules participant visits within protocol-defined windows and optimizes scheduling capacity.
• Performs study‑related procedures, including but not limited to informed consent, screening activities, vital signs, pregnancy tests, height, weight, ECGs, and other protocol‑required assessments.
• Accurately documents participant information and test results as required by the study protocol.
• Maintains investigational product accountability logs when applicable.
• Reports any suspected non‑compliance to appropriate site staff.
• Ensures IRB approval is obtained prior to study initiation and maintained throughout the study.
• Builds positive relationships with participants to support retention efforts.
• Attends study initiation and other relevant meetings for protocol training.
• Conducts participant outreach, appointment scheduling, and follow‑up calls as needed.
• Enters and maintains accurate study data in required systems (e.g., case report forms, EDC) within specified timelines.
• Maintains source documentation, updates participant files, and ensures records are current and complete.
• Follows company policies and standard operating procedures.
• Assists with proper waste disposal and maintains a clean and organized facility as needed.

• BLS certification required.
• Minimum of 2+ years of relevant experience in clinical research or related healthcare setting.

• Strong understanding of the clinical research process, including GCP, SOPs, informed consent, and safety monitoring.
• Ability to work independently with strong attention to detail.
• Capable of analyzing complex information and prioritizing tasks effectively.
• Demonstrated sound judgment and discretion.
• Strong decision‑making, negotiation, and influencing skills.
• Good verbal and written communication skills;
  English fluency preferred.
• Strong organizational and time management skills.
• Proficient in basic computer applications.
• Strong interpersonal skills and ability to work collaboratively in a team environment.