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