Clinical Research Coordinator II

At Headlands Research we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018 our rapidly growing company currently operates 20 sites across the US and Canada with plans for further expansion.

Scottsdale AZ
Headlands Research - Scottsdale
Full-time Onsite (no opportunities for hybrid or remote)

For experienced CRCs looking for stability collaboration and meaningful work

If youre an experienced Clinical Research Coordinator who valuesstrong operations multidisciplinary collaboration and a schedule that actually supports worklife balance Headlands Research - Scottsdale may be the right next step in your career.

Our Scottsdale site is known for its depth of experience thoughtful study execution and team-based approach to clinical researchparticularly in vaccines obesity and weight loss and CNS trials.

About Headlands Research - Scottsdale

Headlands Research Scottsdale is a leading dedicated research center with diverse patient access located just north of the Scottsdale Airport. The Headlands Research Scottsdale team conducts trials in multiple therapeutic areas including but not limited to CNS Psych Musculoskeletal Addiction Healthy Volunteers etc. They are known for their integration of technology to streamline processes for their Sponsor/CRO partners and most importantly subjects.

Why Experienced CRCs Choose Us

• Multi-disciplinary collaborationwith seasoned investigators and clinical staff
• Strong operational support and clear SOPs
• Exposure to complex meaningful studiesnot just high-volume turnover
• Backing of a growing research network with resources and stability

This role is ideal for CRCs who enjoyowning their studies working withcompetent teams and being trusted to execute with precision.

Responsibilities:

• Provide the highest level of care for study patients
• Deliver excellent customer service to pharmaceutical clients
• Coordinate all aspects of assigned clinical trials from site initiation through close-out
• Conduct subject visits and ensure accurate timely documentation in compliance with protocol and standards
• Maintain compliance with protocols GCP/ICH guidelines FDA regulations IRB requirements and SOPs
• Manage subject recruitment informed consent and retention activities
• Ensure timely EDC data entry and resolution of queries
• Report and follow up on AEs SAEs and protocol deviations
• Collaborate with investigators sponsors/CROs labs and internal teams
• Prepare for and participate in monitoring visits audits and inspections
• Maintain regulatory documentation and ensure training compliance for amendments and systems
• Perform study procedures such as phlebotomy ECGs and sample processing (as trained)
• Attend investigator meetings and provide cross-functional support as needed
• Maintain working knowledge of protocols lab manuals equipment calibration and inventory
• Mentor and coach site staff in order to further enhance quality and to best serve our volunteers

Requirements:

• At least 4-5 years of experience managing multiple phase 2-4 industry-sponsored clinical trial studies as the primary coordinator required
• Bachelors degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required.
• Strong understanding of FDA regulations ICH-GCP and clinical trial operations
• Experience with EDC IVRS and clinical research platforms
• Proficiency in medical terminology and clinical documentation
• Strong organizational skills with the ability to manage multiple studies
• Clear professional verbal and written communication skills
• Comfortable working onsite in a collaborative clinical environment

Who Thrives in This Role

• CRCs who wantstructure support and accountability
• Those interested in taking the next step in managing people
• Professionals who valueteamwork over silos
• Coordinators who care about data quality patient experience and compliance
• Those ready to grow within a stable well-established research site

Apply today if youre looking for a CRC role where your experience is respected your schedule is predictable and your work directly contributes to advancing meaningful medical research.