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Investigator Grant Specialist

Novotech
NovoTech
1-3 years
Not Disclosed
India
10 March 19, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Investigator Grant Specialist – Clinical Research & Site Payments

Location: India
Company: Novotech
Employment Type: Full-Time

Job Overview
Novotech is hiring an experienced Investigator Grant Specialist to support clinical trial financial operations, including investigator payments and grant development. This role plays a key part in ensuring accurate budgeting, timely site payments, and compliance with clinical trial agreements and regulatory standards. The ideal candidate will collaborate closely with Project Management and Clinical Operations teams to deliver high-quality financial and operational support across global studies.

Key Responsibilities

Investigator Payment Management

  • Manage and track investigator payments within CTMS, ensuring accuracy and compliance

  • Review site payments against subject visit data to ensure timely and correct disbursement

  • Process site payments quarterly in alignment with contracts and study timelines

  • Identify and escalate payment delays or discrepancies proactively

  • Maintain payment schedules for subject visits based on sponsor and site agreements

  • Prepare and validate site payment reports prior to processing

  • Generate investigator payment reports for study status meetings

  • Ensure audit readiness and compliance with internal SOPs and regulatory requirements

  • Collaborate with Project Managers to address payment-related queries effectively

Clinical Trial Systems & Data Oversight

  • Set up and maintain Subject Visit Tracking (SVT) templates in CTMS

  • Analyze study protocols to configure SVT requirements based on study complexity

  • Ensure accurate and timely system setup for study teams

  • Manage system access and coordinate with vendors for issue resolution

Investigator Grants & Budgeting

  • Develop investigator grants using industry-standard tools such as Grant Plan

  • Review study protocols and collaborate with stakeholders for accurate budget development

  • Provide initial budget estimates and support complex project requirements

  • Apply Fair Market Value (FMV) principles in budget creation

  • Track finalized budgets and ensure accurate reporting

Cross-Functional Collaboration & Compliance

  • Work closely with Clinical Operations, Finance, and Project Management teams

  • Ensure all activities comply with Novotech and client SOPs and guidelines

  • Participate in process improvements, SOP development, and departmental initiatives

  • Maintain professional communication with internal and external stakeholders

Required Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, or a related field

  • Strong understanding of clinical trial processes and investigator payment workflows

  • Proficiency in CTMS (e.g., Veeva) and Grant Plan systems

  • Advanced skills in Microsoft Excel and PowerPoint

  • Excellent analytical, organizational, and problem-solving abilities

  • Strong communication, negotiation, and stakeholder management skills

Experience Required

  • 1–3 years (12–36 months) of experience in a Clinical Research Organization (CRO), pharmaceutical, or healthcare industry

  • Proven experience in investigator payment processing and grant management

  • Hands-on experience with CTMS, subject visit tracking, and clinical budgeting tools

Key Skills

  • Investigator Payments & Budget Management

  • Clinical Trial Financial Operations

  • CTMS & Grant Plan Expertise

  • Subject Visit Tracking (SVT)

  • Data Analysis & Reporting

  • Stakeholder Communication

  • Attention to Detail & Compliance

Why Join Novotech?

  • Work with a globally recognized CRO delivering cutting-edge clinical research solutions

  • Exposure to international clinical trials and advanced financial systems

  • Inclusive and collaborative workplace culture

  • Flexible work environment with wellness and development programs

  • Strong focus on career growth, mentorship, and continuous learning

About Novotech
Novotech is a leading global full-service Contract Research Organization (CRO), delivering clinical development and scientific advisory services to pharmaceutical, biotechnology, and medical device companies. With a strong global presence across Asia-Pacific, the United States, and Europe, Novotech is committed to accelerating innovation and improving patient outcomes worldwide.

How to Apply
Interested candidates can apply through Novotech’s official careers page or submit their updated resume via ThePharmaDaily.com to explore global clinical research opportunities.