Clinical Research Coordinator II – Onsite (Bellingham)

Headlands Research, Inc.; Bellingham (WA); On-site; USD 70,000 - 75,000; Full time

Benefits offered by this job

Health insurance

HSA/FSA

PTO

Disability insurance

Life insurance

401(k) with company match

Job summary

Headlands Research seeks a Clinical Research Coordinator at our Bellingham, WA site. The CRC II will independently manage day-to-day trial conduct, ensuring patient safety, data integrity, and trial enrollment while complying with GCP, FDA, and ICH guidelines.

The role requires 2–5 years of clinical research experience, expertise with EDC/eCRF and CTMS, and a Bachelor’s degree in a relevant field. Onsite work only, with a comprehensive benefits package.

Qualifications

• 2 to 5 years of Clinical Research experience.
• Advanced experience with EDC/eCRF systems and CTMS.
• Ability to manage multiple studies and priorities in a fast-paced environment with minimal supervision.
• Strong attention to detail with high accuracy in documentation.
• Excellent interpersonal, written, and verbal communication skills.
• Bachelor's degree in a scientific/health-related or related field.
• Experience as a Medical Assistant, LPN, or similar clinical background is highly valued.

Responsibilities

• Demonstrates mastery of CRC I responsibilities and performs core coordinator tasks independently.
• Ensures adherence to FDA, GCP, and ICH guidelines and protocols.
• Screens and enrolls study subjects and manages study calendars.
• Collects medical history and adverse events in accordance with protocol.
• Leads trial start-up activities and site initiation activities.
• Ensures accurate data entry in eCRF/EDC systems and maintains ALCOA principles.

Skills

Clinical Research

EDC/eCRF

CTMS

Attention to detail

Communication skills

Education

Bachelor's degree in science/health or related field

Tools

EDC/eCRF systems

CTMS

Job description

Headlands Research seeks a Clinical Research Coordinator at our Bellingham, WA site. The CRC II will independently manage day-to-day trial conduct, ensuring patient safety, data integrity, and trial enrollment while complying with GCP, FDA, and ICH guidelines.

The role requires 2–5 years of clinical research experience, expertise with EDC/eCRF and CTMS, and a Bachelor’s degree in a relevant field. Onsite work only, with a comprehensive benefits package.