Clinical Research Coordinator II

Join Us in Shaping the Future of Clinical Research
Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality safety and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core valuesScientific Rigor Operational Excellence Commitment to Sponsors and Participants and Authentic Collaborationwe create an environment where meaningful work drives meaningful change.

At Adams Clinical youll find:

• A culture of respect transparency and continuous improvement
• Opportunities for professional growth and learning
• A team dedicated to improving lives through innovation and integrity

If youre passionate about making an impact in clinical research and want to be part of a collaborative mission-driven organization wed love to have you on our team.

Overview
Adams Clinical is a rapidly growing research site network specializing focused on late phase industry-sponsored trials of novel treatments for a variety of psychiatric and neurological conditions supporting both inpatient and outpatient studies.

We are seeking experienced applicants for the Clinical Research Coordinator II role at our Watertown location. This role is ideal for coordinators with experience managing one or more trials supporting day-to-day study operations and working collaboratively with research staff under guidance from senior team members.

The Clinical Research Coordinator II independently manages one or more complex or high-enrolling clinical trials within their portfolio. The CRC II is responsible for screening performance study conduct and operational outcomes for assigned studies and may supervise CRC Is or RAs supporting their portfolio. The role requires strong protocol mastery clinical skills and study management capabilities.

Key Responsibilities

• Independently manage a portfolio of complex and/or high-volume trials with guidance from a CRC III or the Site Manager leading all operational and visit-related activities.
• Fully own study execution including screening operations enrollment progress screening vs. target metrics and SCF rates.
• Conduct all participant visits clinical procedures and eligibility assessments per protocol.
• Lead study start-up activities for assigned studies including SIV preparation regulatory readiness supply planning and supporting site completion of required staff training.
• Serve as the primary liaison with study sponsors monitors and CROs.
• Review source and eligibility criteria to ensure accurate screening and enrollment decisions.
• Train and supervise CRC Is or RAs supporting the portfolio; maintain quality and performance oversight.
• Lead data entry and query resolution efforts ensuring high data quality and inspection readiness.
• Maintain investigational product (IP) accountability for assigned studies including receipt storage dispensing reconciliation temperature monitoring documentation and proper disposal ensuring compliance with protocol regulatory requirements and site SOPs.
• Identify operational risks and propose corrective actions to maintain study timelines and quality.
• Compile study metrics across assigned trials including enrollment progress screening performance visit completion and data quality.
• Prepare internal performance summaries for the site team and escalate issues or trends to senior staff.
• Present study metrics and operational updates to sponsors monitors or CRO leadership for assigned trials.
• Serve as a point of contact for resolving data queries and ensuring inspection readiness.

Qualifications

• Bachelors degree required.
• At least 1 year of prior clinical research experience. Experience with industry-sponsored clinical trials required.
• Demonstrated ability to manage complex studies independently.
• Strong communication skills and comfort interacting directly with sponsors.

Pay: $32.00 - $36.00 per hour

• 401(k) matching
• Medical Dental & Vision insurance
• Employee assistance program
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Parental leave
• Professional development assistance

Adams Clinical is committed to being an equal opportunity and affirmative action employer. We focus on hiring and nurturing top talent. All employment decisions including recruitment hiring promotion compensation transfer training discipline and termination are made based on the candidates or employees qualifications relevant to the position. These decisions are made without regard to age sex sexual orientation gender identity or expression genetic information race color creed religion ethnicity national origin citizenship disability marital status military status pregnancy or any other legally protected status.

In compliance with federal law all individuals hired must as a condition of employment provide documentation verifying their identity and authorization to work in the United States and complete Form I-9 within the requiredtimeframe. Adams Clinicalparticipatesin E-Verify to confirm employment eligibility.