Senior Manager, Investigator Grants

The Senior Manager, Global Investigator Grants leads the global grants team responsible for processing investigator site payments through the Clinical Trial Management System (CTMS), ensuring payments are accurate, timely, and in accordance with the financial terms of the Clinical Trial Agreement. This role serves as the financial lead on project teams for site payments, providing oversight of payment processing, advance reconciliations, and month-end reporting. The position is heavily client facing, partnering directly with clients to review monthly investigator grant results, accruals, forecasting, and change order budgets.

As the Global Investigator Grants liaison with Business Operational Excellence, the Senior Manager will play a key role in the implementation of the CTMS Site Payment Module, including data validation, system setup, and the development of training materials, and will transition the team to processing site payments in the CTMS. This role is critical to strengthening process efficiency, internal controls, and the overall site payment experience for Precision, our clients, and investigator sites.

Main Duties and Responsibilities:

• Serves as the financial lead on the Project Team for site payments on a global basis, ensuring investigator payments are processed through the CTMS in accordance with the financial terms of the Clinical Trial Agreement (CTA)

• Leads the global grants team responsible for site payment processing in the CTMS, including, but not limited to: timely and accurate investigator payments, advance (pre-paid funds) balance reconciliations, and reporting

• Serves as the Global Investigator Grants liaison with Business Operational Excellence for the implementation of the CTMS Site Payment Module, including data validation, system setup, and the development of training materials, and leads the team's transition to processing site payments in the CTMS

• Oversees the setup and maintenance of site payment terms in the CTMS on a global basis, interpreting the financial section of the CTA to ensure payment schedules are configured accurately and payments are processed timely

• Responsible for contributing to the month-end close process by generating a global report from the CTMS on a project-by-project basis inclusive of, but not limited to: amounts invoiced/paid, advance balances remaining, prepaid balance analysis, projections, and other key performance indicators as applicable

• Works with the respective Project Directors and Project Managers to provide guidance on the financial section of the Clinical Trial Agreement

• Works with the respective Project Directors and Project Managers to ensure visits and other payment-eligible activities are accurately captured in the CTMS so they can be tracked and paid; provides training as applicable

• Ensures site payments processed in the CTMS meet the terms and conditions of the Clinical Trial Agreement, with appropriate review, approval, and internal controls

• Responsible for overseeing the Sunshine Act Reporting process and other client reporting as applicable on a global basis, leveraging CTMS payment data

• Serves in a heavily client-facing capacity, leading regular client meetings to review monthly investigator grant results, accruals, forecasting, and change order budgets; participates in internal team calls and Quarterly Business Review Meetings as applicable

• Other duties as assigned by manager

Minimum Education and Experience:

• Minimum of bachelor's degree in business administration, Accounting, Finance or similar field

• Minimum of 5 years of CRO experience or equivalent relevant experience and/or demonstrated competencies in the key requirements of the role

• Experience implementing the site payment module within a Clinical Trial Management System (CTMS), including data validation, system setup, and user training; experience with Veeva Vault CTMS preferred

• Minimum of 3 years of managing direct reports

Knowledge, Skills, and Competencies:

• Experience with clinical trial payment process, internationally

• Experience with clinical trial agreements and site budgets

• Strong understanding of the study start-up process

• Strong analytical skills

• Excellent time management skills

• Analyze, reconcile, and communicate financial results with all levels of project team, investigator sites, and clients.

• Strong working knowledge of the grant administration and site contracting process on a global basis with the ability to thrive  in a multi-tasking environment

• Strong financial and analytical skills.

• High energy and enthusiasm with a strong commitment to exceeding expectations.

• Flexibility and willing to work on multiple assignments of varying tasks with personnel throughout the organization.

• Ability to learn quickly in order to make an immediate impact and provide value-added services throughout the organization and with our clients.

• Strong communication & interpersonal skills, displaying the ability to connect and build relationships with management and others throughout the organization.

• Exhibits high self-motivation, and is able to work and plan independently as well as in a team environment.

• Team player with a strong desire to be an active, long-term participant in the growth of the company.

• Focuses on continuous improvement, including the ability to make proactive assessments on how to make processes more efficient while enhancing internal controls.

#LI-REMOTE

Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case.  This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.
Reasonable estimate of the current range
$121,800 — $152,200 USD

Any data provided as a part of this application will be stored in accordance with our  Privacy Policy.  For CA applicants, please also refer to our  CA Privacy Notice .

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected] .

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [email protected] so we can investigate and take appropriate action.

Candidates must be legally authorized to work in the country of employment without employer sponsorship.