Investigator Grants Specialist - Argentina

Premier Research International; Argentina; On-site; ARS 92,724,000 - 154,540,000; Full time

Job summary

Premier Research International in Argentina is seeking an Investigator Grants Specialist to join our Clinical Strategy and Business Operations team. You will help biotech and pharma partners translate ideas into medicines and devices while supporting budgets and grant processes.

You will collaborate with internal stakeholders to prepare investigator budgets, ensure FMV compliance, and provide estimates based on available protocol information.

Qualifications

• Undergraduate degree in sciences or related field.
• Two years of Clinical Research site, data management, clinical operations, or start-up experience.
• One year of contracts and/or grant management experience.
• Strong analytical and problem-solving skills.
• Advanced computer skills with Excel and Word.
• Critical thinking to identify effective and efficient solutions.

Responsibilities

• Prepare moderately complex investigator budgets to support new business opportunities according to fair market value.
• Collaborate with the operational and proposals teams to meet deadlines and ensure budget development.
• Support BD and operations to provide required investigator fee estimates for proposals.
• Interpret protocol information to develop investigator budgets per FMV and regulatory guidance.
• Provide estimates for projects with limited customer information using experiential data.
• Develop site budget estimates by country per feasibility specs and FMV costs.
• Maintain high-quality investigator pricing budgets aligned with timelines and standards.

Skills

Analytical skills

Problem-solving

Critical thinking

Education

Undergraduate degree in sciences

Tools

Microsoft Office

Excel

Word

Job description

Premier Research is looking for a Investigator Grants Specialist - Argentina to join our Clinical Strategy and Business Operations team.

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.

Your ideas influence the way we work, and your voice matters here.

As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.

What you'll be doing:

• Prepare moderately complex investigator budgets to support the acquisition of new business in accordance with fair market value regulations
• Collaborates with the operational and proposals team, along with any other internal stakeholders, to meet deadlines and ensure appropriate budget development
• Support Business Development and operational contacts to provide required investigator fee estimates for inclusion in proposal budgets
• Interpret with support, study synopsis, draft protocol, or final protocol, where available, to develop investigator budgets in accordance with fair market value
• Provide estimations with support, on projects, where minimal information is available from the customer, based on experiential and historical data in similar projects
• With limited supervision, develops investigator site budget estimates for each country, per feasibility specifications, according to available protocol information and fair market value costs and regulations (i.e. Medicare and Medicaid Affordability Act (Sunshine Act, etc.)
• Maintains the quality of the investigator pricing budget generated for internal/external protocols, ensuring that it is prepared in a cost-effective manner, meeting agreed timelines and expectations and in accordance with industry/ internal regulations and quality standards

What we're searching for:

• Undergraduate degree or its international equivalent preferably in the Sciences or in a related field from an accredited institution
• Two years of Clinical Research site, data management, clinical operations, or start-up experience in the Pharmaceutical, Biotech, Medical Device industry
• One year of contracts and/or grant management experience
• Strong analytical and problem-solving skills
• Advanced computer skills with Microsoft Office suite, including Excel and Word
• Critical thinking skills to identify effective and efficient solutions for complex problems and determine opportunities for improvement