Project Manager II, Translational Neuroscience - cm

American Addiction Centers • Winston-Salem, NC

1d • $33 - $50 • Hybrid

About The Position

We are seeking a highly motivated and skilled Project Manager to join our research team. This role requires a self-motivated, proactive leader who will be providing independent oversight and execution of funded research operations. This role is responsible for ensuring study objectives are met within established timelines, budgets, and regulatory requirements while proactively driving progress across all phases of research.

Requirements

• NC Driver's license is required.
• A valid North Carolina driver’s license is required.

Responsibilities

• Independently oversee the enrollment activities and day-to-day work of Clinical Study Coordinators (CSCs), ensuring alignment with study goals and timelines.
• Lead end-to-end management of participant engagement, ensuring timely study completion, accurate data collection, and participant compensation.
• Exercise independent judgment to monitor and optimize participant flow and study processes to ensure successful completion within grant budgets.
• Draft and contribute to progress reports and research documentation for NIH and other external stakeholders with minimal supervision.
• Partner strategically with the Program Manager through regular meetings to evaluate study progress, identify challenges, and develop next steps for publications and future studies.
• Direct and execute research activities in accordance with study protocols, including recruitment, eligibility screening, data collection, and quality assurance.
• Independently coordinate regulatory processes, including preparation and dissemination of materials, and lead training efforts for study staff and graduate students.
• Maintain active involvement in research execution, including participant interaction, data collection, and contributing as a collaborative team member.
• Provide guidance and mentorship to CSCs and study staff, offering support as needed while encouraging independent performance and accountability.
• Proactively assist less experienced staff in meeting recruitment and screening targets, ensuring protocol adherence and study efficiency.
• Oversee and support participant consent processes, screenings (including telephone screenings), and study visits.
• Conduct participant sessions, including administration of questionnaires, psychological interviews, data collection, and sample processing.
• Independently review and monitor documentation of adverse events, ensuring compliance with regulatory standards.
• Maintain comprehensive knowledge of applicable regulatory requirements and ensure ongoing adherence.
• Manage study supply inventory and ordering as needed with minimal oversight.
• Collaborate with the Program Manager and Principal Investigator (PI) to evaluate recruitment progress and refine strategies to meet or exceed study goals.
• Independently assess data quality and implement corrective actions as needed.
• Analyze study coordinator schedules and enrollment data to identify opportunities to improve enrollment efficiency, diversity, and inclusion.
• Take initiative in expanding responsibilities to support evolving research programs, particularly in neuroscience clinical trials.
• Contribute to both research and administrative functions, demonstrating adaptability and ownership of program success.

Benefits

• Paid Time Off programs
• Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
• Flexible Spending Accounts for eligible health care and dependent care expenses
• Family benefits such as adoption assistance and paid parental leave
• Defined contribution retirement plans with employer match and other financial wellness programs
• Educational Assistance Program

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed