About The Role:
Job Summary
The Senior Investigator Grant Specialist is responsible for the development, negotiation, and management of investigator grants and site payments for global clinical trials. This role serves as a subject matter expert (SME) within the Investigator Grants & Payments function, liaising with Clinical Operations, Contracts, Finance, and Investigative Sites to ensure budgets and payments are accurate, compliant, and delivered within agreed timelines.
The role also supports process improvements, operational excellence initiatives, and mentoring of junior team members.
Minimum Qualifications & Experience
Bachelor's degree in Life Sciences or a related field.
5+ years of experience within a CRO, pharmaceutical, biotechnology, or related clinical research environment.
Experience in investigator budget development. Experience working on a budget development tool such as GrantPlan is highly desired.
Experience in investigator payments and site reimbursement processes. Must have experience working in CTMS/Veeva.
Must have analytical, problem solving skills.
Excellent verbal and written communication and negotiation skills.
Excellent interpersonal and relationship building skills.
Extremely well organized and detailed oriented.
Roles and Responsibilities
Investigator Grants & Budget Management
Develop and negotiate investigator site budgets based on study protocols, Schedule of Assessments (SOA), and sponsor requirements.
Conduct protocol reviews to identify billable procedures, budget drivers, and payment milestones.
Perform budget benchmarking and Fair Market Value (FMV) assessments.
Develop country-specific and site-specific budget templates, where applicable.
Manage budget-related queries, escalations, and stakeholder communications.
Ensure budget assumptions are documented, justified, and aligned with sponsor expectations.
Investigator Payment Management
Manage the end-to-end investigator payment lifecycle for assigned studies.
Review and maintain payment schedules in accordance with executed agreements and approved budgets.
Generate, validate, reconcile, and process investigator payments within established timelines and SLAs.
Reconcile payment data across CTMS, EDC, contracts, study trackers, and related systems.
Monitor held, overdue, or disputed payments and drive timely resolution.
Investigate and resolve payment discrepancies, missing data, and system-related issues.
Support payment forecasting and reporting activities.
Collaborate with Clinical Operations, Project Management, Contracts, Finance, CRAs, and investigative sites to resolve issues and support study delivery.
Additional Responsibilities
Act as an SME for investigator grants and payment processes.
Serve as the primary point of contact for complex investigator grant and payment-related matters.
Identify opportunities to improve processes, controls, templates, systems, and automation initiatives.
Contribute to SOPs, work instructions, training materials, and departmental continuous improvement activities.
Provide guidance, mentoring, and training to junior team members.
Support onboarding and knowledge-sharing initiatives across the team.
Ensure compliance with company SOPs, study agreements, regulatory requirements, and client expectations.
Maintain audit-ready documentation and support audits, inspections, and quality reviews.
Ensure adherence to departmental KPIs, quality standards, and service-level agreements.
Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect. Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.
We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.
We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application.
Roles and Responsibilities
Investigator Grants & Budget Management
Develop and negotiate investigator site budgets based on study protocols, Schedule of Assessments (SOA), and sponsor requirements.
Conduct protocol reviews to identify billable procedures, budget drivers, and payment milestones.
Perform budget benchmarking and Fair Market Value (FMV) assessments.
Develop country-specific and site-specific budget templates, where applicable.
Manage budget-related queries, escalations, and stakeholder communications.
Ensure budget assumptions are documented, justified, and aligned with sponsor expectations.
Investigator Payment Management
Manage the end-to-end investigator payment lifecycle for assigned studies.
Review and maintain payment schedules in accordance with executed agreements and approved budgets.
Generate, validate, reconcile, and process investigator payments within established timelines and SLAs.
Reconcile payment data across CTMS, EDC, contracts, study trackers, and related systems.
Monitor held, overdue, or disputed payments and drive timely resolution.
Investigate and resolve payment discrepancies, missing data, and system-related issues.
Support payment forecasting and reporting activities.
Collaborate with Clinical Operations, Project Management, Contracts, Finance, CRAs, and investigative sites to resolve issues and support study delivery.
Additional Responsibilities
Act as an SME for investigator grants and payment processes.
Serve as the primary point of contact for complex investigator grant and payment-related matters.
Identify opportunities to improve processes, controls, templates, systems, and automation initiatives.
Contribute to SOPs, work instructions, training materials, and departmental continuous improvement activities.
Provide guidance, mentoring, and training to junior team members.
Support onboarding and knowledge-sharing initiatives across the team.
Ensure compliance with company SOPs, study agreements, regulatory requirements, and client expectations.
Maintain audit-ready documentation and support audits, inspections, and quality reviews.
Ensure adherence to departmental KPIs, quality standards, and service-level agreements.
Minimum Qualifications & Experience
Bachelor's degree in Life Sciences or a related field.
5+ years of experience within a CRO, pharmaceutical, biotechnology, or related clinical research environment.
Experience in investigator budget development. Experience working on a budget development tool such as GrantPlan is highly desired.
Experience in investigator payments and site reimbursement processes. Must have experience working in CTMS/Veeva.
Must have analytical, problem solving skills.
Excellent verbal and written communication and negotiation skills.
Excellent interpersonal and relationship building skills.
Extremely well organized and detailed oriented.
Novotech is a global full-service clinical Contract Research Organization (CRO).
At Novotech, ambition meets opportunity. As a globally recognized leader in clinical research and scientific advisory services, we are proud to combine our position at the forefront of the industry with an award-winning workplace culture that values ambition, innovation, and growth. Named Employer of Choice, Great Place to Work and Employer of Choice for Gender Equality (EOCGE), we are committed to fostering an environment that reflects the life-changing work we do.
Since 1997, we have expanded our global footprint, now with 30+ offices across Asia-Pacific, the United States, and Europe. This growing network unites professionals from diverse backgrounds and disciplines to advance therapies that improve patient outcomes worldwide.
At Novotech, our employees are at the heart of our success. By offering trust, flexibility, and autonomy through programs like NovoLife, our flexible benefits framework, we empower team members to create an effective work-life balance that delivers professional satisfaction and maximum results for clients.
With access to mentorship opportunities, professional development programs, and a dynamic community, Novotech offers a platform for driven individuals to achieve personal growth while shaping the future of healthcare. Join us to be a part of a team that values your contributions and supports your ambition to make a global impact.
At Novotech we have advanced therapeutic and regulatory expertise, the ability to execute across markets and a client-centric service model, so that our clients get a trusted, long-term partner and an accelerated path to bring their life-changing advances to market. This gives our employees the opportunity to develop their careers by joining a diverse and supportive global organization with a collaborative culture, whilst working with clients on the cutting-edge of life sciences.
At Novotech you will work alongside empowered teams with a shared commitment to success.
- Strategic vs transactional mindset.
- Ability to gain insights and make proactive decisions quickly.
- Culture that fosters partnership and collaboration, where every voice is heard and valued.
- Ongoing support from senior stakeholders and leadership team.
