CRC II: Neuro & Psych Clinical Trials Lead

Adams Clinical, Inc.; DeSoto (TX); Presencial; USD 34 000 - 41 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

401(k) matching

Employee assistance program

Flexible spending account

Health insurance

Health savings account

Life insurance

Paid time off

Parental leave

Resumo da oferta

Adams Clinical is seeking an experienced Clinical Research Coordinator II at our Dallas location. This role is ideal for coordinators who can manage more than one trial, supervise others, and support day-to-day operations across inpatient and outpatient studies in psychiatric and neurological conditions.

You will independently oversee screening, enrollment metrics, visits, regulatory readiness, IP accountability, start-up activities, and serve as a primary liaison with sponsors, monitors, and

Qualificações

• At least 1 year of experience as a CRC on industry-sponsored trials.
• Experience with neuro and/or psych patient populations is a plus.
• Ability to manage complex studies independently.
• Comfortable with 12-20 participant visits per day.
• Strong communication with sponsors.

Responsabilidades

• Manage a portfolio of complex and/or high-volume trials with guidance from senior staff.
• Own study execution including screening, enrollment progress, metrics.
• Conduct participant visits, procedures, and eligibility per protocol.
• Lead start-up activities: SIV prep, regulatory readiness, training.
• Serve as primary liaison with sponsors, monitors, CROs.
• Train and supervise CRC I's or RAs.
• Lead data entry and query resolution to ensure data quality.
• Maintain IP accountability: receipt, storage, dispensing, reconciliation, temperature monitoring, disposal.

Conhecimentos

Clinical research coordinator经验

Neuro/psych population experience

Independent study management

High patient visits

Sponsor communication

Descrição da oferta de emprego

Adams Clinical is seeking an experienced Clinical Research Coordinator II at our Dallas location. This role is ideal for coordinators who can manage more than one trial, supervise others, and support day-to-day operations across inpatient and outpatient studies in psychiatric and neurological conditions.

You will independently oversee screening, enrollment metrics, visits, regulatory readiness, IP accountability, start-up activities, and serve as a primary liaison with sponsors, monitors, and