Clinical Contracts Project Manager I - NCCT

American Addiction Centers; United States; Remote; USD 39,000 - 59,000; Full time

Benefits offered by this job

Fully remote

Job summary

American Addiction Centers through the NCCT Administration is seeking a highly organized professional to manage intake and documentation for non-federal clinical research studies, ensuring smooth progression from sponsor contact to study start-up. The role involves budget development and contract coordination to support efficient execution.

This fully remote, full-time position operates during normal business hours Monday–Friday, with benefits eligibility and a focus on clinical trial workflows

Qualifications

• Experience in research administration and clinical trial workflows.
• Budget development and trial management builds.
• Contract coordination and sponsor communication.

Responsibilities

• Manage intake and document coordination for all non-federal studies.
• Oversee initiation and budget development for study start-up.
• Coordinate contracts with sponsors and OCR Pre-Award Team.

Skills

Research administration

Clinical trial workflows

Budget development

Contract coordination

Job description

Department:

10010 NCCT (National Center for Clinical Trials) - Administration

Status:

Full time

Benefits Eligible:

Yes

Hou** rs Per Week:

40

Schedule Details/Additional Information:

• Fully Remote




• Normal business hours, Monday-Friday

Pay Range:

$28.55 - $42.85

The National Center for Clinical Trials (NCCT) is designed to serve as an innovative platform to revolutionize and catalyze the conduct of clinical trials- greatly accelerating the translation of scientific findings into improvements in the prevention, diagnosis, and treatment of disease for our communities and patients. The NCCT will offer core services for patient recruitment and enrollment, trial administration and follow-up, and to gather real world data and evidence.

This position will be part of a team that will report to leadership in the NCCT and will manage the intake, document coordination and overall initiation of all non-federal clinical research studies submitted through the NCCT to the Office of Clinical Research (OCR) Pre-Award Team. This position ensures projects progress efficiently from initial sponsor contact through study start-up, including budget development, trial management builds, and contract coordination. The ideal candidate is highly organized, tech-savvy, and experienced in research administration and clinical trial workflows.