Manager, Global Investigator Grants (LATAM)

We’re expanding across  Mexico, Brazil, Argentina, Colombia, Chile, and Peru , and we’re looking for an Investigator Grants Team Manager to lead our new team in LATAM!

As the Manager of our Global Investigator Grants Team you will lead the development of investigator grant/site budgets during the proposal process while supporting revision generation and contribute to the clinical trial budgets finalization process. Manage and oversee the clinical site budgeting tools leveraging your background with complex protocol modeling and site budget experience.

Essential functions of the job include but are not limited to:

Serves as a financial lead on the Project Team from a grant administration perspective on a global basis

Oversees the grant administration team which includes, but not limited to: budget management  and maintenance, timely and accurate investigator payment processing, advance (pre paid  funds) balance reconciliations, and reporting

Responsible for overseeing the creation of the investigator grant workbooks on a global basis which entails interpreting the financial section of the Clinical Trial Agreement (CTA) in order to facilitate and timely and accurate payment process

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

Work with the respective Project Directors and Project Managers in order toprovide guidance on the financial section of the Clinical Trial Agreement

Work with the respective Project Directors and Project Managers in order to provide guidance on how to populate the site payment workbook to ensure visits eligible for payment are tracked and processed; provide training as applicable

Responsible for overseeing the Sunshine Act Reporting process and other client reporting as applicable on a global basis

Responsible for the management and processing of payments to the sites as per the terms and conditions of the Clinical Trial Agreement

Participate in internal team calls, client calls, and Quarterly Business Review meetings as required

Qualifications:

Minimum Required:

Minimum of a Bachelor's degree in Business Administration, Accounting, Finance and/or equivalent in a similar field

Minimum of 5 years of Clinical Research experience or equivalent relevant experience 

Minimum of 3 years of experience in a leadership role

Other Required:

No routine travel is expected for this position; however, occasional travel domestically or internationally may be required

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

Preferred:

Ability to drive and meet critical deadlines

Strong proficiency in Microsoft Excel

Excellent communication skills, both verbal and written

Extremely detailed oriented and process driven

Fluency in English and for non-English speaking countries the local language of country where position based

Competencies:

Strong working knowledge of the grant administration and site contracting process on a global basis with the ability to thrive in a matrix 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-AG2 #LI-REMOTE

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 myHR@precisionmedicinegrp.com .

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 myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.