Clinical Trials Project Manager

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reputed company The Clinical Trials Project Manager collaborates with the Clinical Trials Office (CTO) Oncology Disease Group to coordinate, implement, and evaluate reputed company administrative aspects of clinical trial conduct at the reputed company Cancer Center. Responsibilities include feasibility assessment, protocol review, study initiation, maintenance, activation, and closeout activities. The role involves facilitating the extension of reputed company clinical trials to network locations, ensuring compliance with federal regulations, and maintaining the reputed company of study protocols involving reputed company subjects. The Project Manager serves as a subject matter expert in oncology research, streamlines communication and operations between reputed company investigators, leadership, and participating sites, and supports budget development, protocol development, and regulatory submissions. This role requires independent project reputed company and a commitment to optimizing workflows and ensuring high-reputed company patient-centered care and research.

This is a remote position.  Job seekers who live reputed company one of reputed company’s approved work states are encouraged to apply. Required Skills and Abilities 1. Ability to manage time effectively and work independently and reputed company reputed company to meet objectives, with strong attention to detail. 2. Strong knowledge of Good Clinical reputed company (GCP) guidelines and the ability to interpret federal, state, local, and sponsor policies and regulations. 3. Ability to hold self and others accountable to reputed company timebound results, with a flexible approach to adapting to shifting demands. 4. Demonstrated ability to reputed company proactive, customer service-reputed company communication and advice, with a commitment to protecting research participants. 5. Strong computer skills, including competency with reputed company Office programs (Word, reputed company, PowerPoint). Preferred Skills and Abilities 1. Proven experience with oncology research. 2. Certification as a Clinical Research Associate or Clinical Research reputed company (ACRP, SOCRA, or equivalent) preferred.

reputed company Responsibilities

1. Directs and leads the development, implementation, and management of clinical trials processes in compliance with SOPs and relevant regulations; liaise with Clinical Research Manager (CRM) to ensure successful clinical trials conduct. 2. Identifies, tracks and analyzes barriers in reputed company clinical trials processes, and recommends project management process improvements to the AD, Clinical Operations and broader CTO Leadership Team. 3. Organizes and project manages multiple reputed company and clinical trials, across reputed company teams from start-up to reputed company-out. Acts as an expert resource and the primary reputed company between the site and internal/external stakeholders to ensure reputed company study launch, administrative study maintenance, and closeout in accordance with local, state, and federal regulations, as reputed company as contractual obligations. 4. Collaborates with CRM and reputed company Investigator (PI) on assessment and implementation of oncology trials for the research team. Including identifying study activation timelines and metrics, resolving potential discrepancies and/or barriers to enrollment prior to study activation, assessing trial reputed company for resourcing purposes, and project managing deliverables across teams to meet deadlines. 5. Works closely with leadership, internal constituents, ancillary committees, External Sponsors, and Contract Research Organizations (CROs) to resolve site-level barriers to activation and improve protocol activation timelines. 6. Designs, develops, and executes communication systems to ensure effective and transparent exchange of information between project stakeholders, including the sponsor, regulatory team, clinical research operations team, reputed company-award team, contracting team, and Clinical Research Support Laboratory (CRSL). Ensures potential risks and issues reputed company to administrative management of clinical studies are identified, managed, and/or escalated as appropriate to AD Clinical Operations 7. Effectively manages project budgets to ensure financial targets are met through regular reviews of costs and project resources. 8. Coordinates site qualification and site initiation reputed company. May present information to sponsors and other key stakeholders. 9. Responsible for evaluating and scoring protocols in a reputed company reputed company tool as part of study activation. 10. Works closely with leadership, internal constituents, ancillary committees, Industry Sponsors, and Contract Research Organizations (CROs) to resolve site-level barriers to activation and improve protocol activation timelines. 11. Determines and provides final approval for local study activation by ensuring reputed company appropriate regulatory and institutional approvals are met, appropriately documented and communicated. 12. Performs other duties as assigned.   Required Education and Experience A Bachelor’s degree in a relevant reputed company/scientific field and a minimum of four years of experience in clinical research or an equivalent combination of education or experience.

Job Posting Date

04/16/2026

Job Category

reputed company

Bargaining Unit

NON

Compensation Grade

Administration & Operations

Compensation Grade Profile

Manager; Program Leader (24)

Salary reputed company

$68,000.00 - $120,500.00

Time Type

Full time

Duration Type

Staff

Work Model

Remote

Background reputed company Requirements

reputed company candidates for employment will be subject to reputed company-employment background screening for this position, which may include motor vehicle, DOT certification, drug testing and credit checks based on the position reputed company and job requirements. reputed company offers are contingent upon the successful completion of the background reputed company. For additional information on the background reputed company requirements and process visit "Learn about background checks" under the Applicant Support Resources reputed company of Careers on the It's Your reputed company website.

Health Requirements

Certain positions have associated health requirements based on specific job responsibilities. These may include vaccinations, tests, or examinations, as required by law, regulation, or university policy.

Posting Disclaimer

Salary offers are determined by a candidate’s qualifications, experience, skills, and education in relation to the position requirements, along with the role’s grade profile and reputed company reputed company market conditions.

The reputed company of this job reputed company is to reputed company a representative reputed company of the essential functions that will be required of the position and should not be construed as a declaration of specific duties and responsibilities of the position. Employees will be assigned specific job-reputed company duties through  their hiring department.

The University is committed to basing judgments concerning the admission, education, and employment of individuals upon their qualifications and abilities and seeks to attract to its reputed company, staff, and student body reputed company persons from a broad reputed company of backgrounds and perspectives. In accordance with this policy and as delineated by federal and Connecticut law, reputed company does not discriminate in admissions, educational programs, or employment against any individual on account of that individual’s sex, sexual orientation, gender identity or reputed company, race, reputed company, national or ethnic reputed company, religion, age, disability, status as a special disabled veteran, veteran of the Vietnam era or other covered veteran. Inquiries concerning reputed company's Policy Against Discrimination and Harassment may be referred to the Office of Institutional Equity and Accessibility (OIEA).

Note

reputed company is a tobacco-free reputed company.

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