Medpace is hiring experienced professionals for five clinical research and pharmaceutical industry roles in India. Current Medpace openings include SAS Programmer, Site Payments Processor, Experienced SAS Programmer, Regulatory Submissions Coordinator, and Study Start-up Submissions Manager.

The opportunities are primarily based in Navi Mumbai, while the Study Start-up Submissions Manager position is remote-based in Delhi. Candidates from Life Sciences, Statistics, Mathematics, Health Informatics, Data Science, Computer Science, Science, Finance, Accounting, Business and related disciplines may be eligible depending on the position.

These Medpace jobs are particularly relevant for professionals seeking careers in clinical SAS programming, biostatistics, clinical operations, site payments, regulatory submissions, CDSCO/DCGI submissions and clinical trial start-up.

Medpace Hiring 2026 – Job Overview

1. SAS Programmer – Navi Mumbai

Department: Biostatistics
Job ID: 12315
Location: Navi Mumbai, India
Employment Type: Full-time, Office-based
Experience: SAS knowledge required; 1–2 years preferred

Medpace is seeking an SAS Programmer to join its Biostatistics team. This position is suitable for candidates with SAS programming knowledge who want to develop their careers in clinical research and biostatistics.

Responsibilities

• Write SAS programs to create analysis datasets.
• Generate tables, listings and figures using SAS.
• Program, validate and maintain mapped databases.
• Develop edit checks for external clinical data.
• Work with Data Management teams on database specifications.
• Coordinate data-transfer requirements and resolve data-related issues.

Qualifications

Candidates should have a Bachelor’s or Master’s degree in one of the following or a closely related discipline:

• Mathematics
• Statistics
• Health Informatics
• Data Science
• Computer Science
• Life Sciences

SAS Certification is required. Candidates should possess SAS knowledge, with 1–2 years of experience preferred, along with good written and verbal English communication skills.

2. Site Payments Processor – Navi Mumbai

Department: Site Activation & Maintenance
Job ID: 12313
Location: Navi Mumbai, India
Employment Type: Full-time, Office-based
Experience: 1+ year

The Site Payments Processor will support Medpace’s Clinical Operations team by managing site payment processing, accounts payable activities, invoice reconciliation and study-related financial records.

Responsibilities

• Execute accounts payable and site-payment data-entry activities.
• Configure system requirements for tracking and administering site payments.
• Process and calculate clinical trial site payments.
• Prepare project and site reports.
• Coordinate site-specific agreements and amendments.
• Map site payees within payment systems.
• Code, track and reconcile site invoices against relevant data sources.

Qualifications

Candidates should have:

• Bachelor’s degree in a related discipline.
• At least 1 year of related experience in finance, treasury, accounting or a business-related field.
• Proficiency in Microsoft Office.
• Strong organizational and time-management skills.
• Ability to prioritize tasks and meet deadlines.
• Excellent attention to detail.
• Professional approach when handling confidential information.

3. Experienced SAS Programmer – Navi Mumbai

Department: Biostatistics
Job ID: 12319
Location: Navi Mumbai, India
Employment Type: Full-time, Office-based
Experience: 5+ years

Medpace is also hiring experienced SAS professionals for its Biostatistics team. This senior-level opportunity requires extensive SAS programming expertise and strong knowledge of clinical research data standards.

Responsibilities

• Develop specifications for new clinical research projects.
• Serve as a project team leader when required.
• Write SAS programs for analysis datasets, tables, listings and figures.
• Set up, validate and maintain mapped databases.
• Integrate external clinical data.
• Develop and validate external-data edit checks.
• Independently produce high-quality SAS programming outputs.
• Support database validation and maintenance activities.

Qualifications

Applicants should possess a Bachelor’s or Master’s degree in:

• Mathematics
• Statistics
• Health Informatics
• Data Science
• Computer Science
• Life Sciences

Additional requirements include:

• 5+ years of SAS programming experience.
• Excellent knowledge of CDISC standards.
• SAS Certification.
• Thorough understanding of the pharmaceutical industry.
• Knowledge of regulations governing electronic records.
• Strong analytical skills.
• Excellent written and verbal communication skills.

4. Regulatory Submissions Coordinator – Senior/Experienced

Department: Site Activation & Maintenance
Job ID: 12919
Location: Navi Mumbai, India
Work Mode: Office-based with hybrid arrangements subject to eligibility
Experience: More than 4 years

This Medpace regulatory submissions job is intended for experienced clinical research professionals with hands-on knowledge of Ethics Committee, CDSCO and DCGI regulatory submissions.

Responsibilities

• Conduct activities required for investigative-site activation.
• Prepare, review and submit documentation to Regulatory Agencies.
• Communicate study progress with global study teams.
• Identify risks affecting site activation and develop mitigation strategies.
• Guide study teams regarding ethics and regulatory submissions.
• Review and finalize essential site-activation documents.
• Serve as a primary contact for regulatory and ethics submission activities.
• Communicate directly with investigative sites.
• Ensure regulatory submissions comply with applicable regulations and guidance.
• Advise sponsors regarding changing regulatory requirements.
• Track submissions and ensure timely filing of documents.

Qualifications

Candidates should have:

• Bachelor’s degree in a Science field.
• More than 4 years of regulatory submissions experience in clinical research.
• CRO experience is preferred.
• Hands-on experience preparing, reviewing and submitting documentation to Ethics Committees and Regulatory Authorities.
• Practical experience with CDSCO and DCGI submissions.
• Experience preparing responses to regulatory queries.
• Strong written and verbal communication skills.

Candidates willing to travel to Delhi when required may have an advantage.

Strong local regulatory experience is mandatory for the Regulatory Submissions Coordinator level. Local and regional APAC experience is required for Regulatory Submissions Manager-level responsibilities.

5. Study Start-up Submissions Manager – Delhi

Department: Site Activation & Maintenance
Job ID: 12312
Location: India – Remote-based in Delhi
Experience: More than 8 years

The Study Start-up Submissions Manager will oversee local and regional APAC clinical trial start-up and regulatory submission activities. The position requires substantial experience working with Indian regulatory authorities, including CDSCO and DCGI.

Responsibilities

• Closely follow up on clinical trial applications submitted to DCGI.
• Conduct face-to-face visits when required.
• Facilitate meetings and consultations with DCGI.
• Manage local and regional APAC study start-up activities.
• Independently communicate with sponsors, investigative sites, IRBs, Ethics Committees and regulatory agencies.
• Perform quality checks of submission and essential site documents.
• Prepare and approve informed consent forms.
• Monitor regulations and develop solutions to study start-up challenges.
• Participate in bid defenses, capabilities meetings and audits.

Qualifications

Candidates should have:

• Bachelor’s degree.
• More than 8 years of regulatory submissions experience in clinical research, preferably within a CRO.
• Relevant CRA or project-management experience may also form part of the candidate’s background.
• Strong local regulatory experience.
• Regional APAC experience for Regulatory Submissions Manager-level positions.
• Hands-on experience preparing, reviewing and submitting documentation to Ethics Committees and Regulatory Authorities.
• Experience formulating responses to regulatory queries.
• Excellent oral and written communication skills.

Who Can Apply for Medpace Jobs?

Depending on the specific vacancy, candidates with the following educational backgrounds may be considered:

B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Mathematics, Statistics, Life Sciences, Health Informatics, Data Science, Computer Science, Finance, Accounting, Business and other relevant Bachelor’s/Master’s degrees.

However, applicants should carefully match their qualification and professional experience against the requirements of the individual role. For example, SAS Programmer positions specifically require SAS expertise, while senior regulatory roles require substantial hands-on clinical research regulatory submission experience.

Why Join Medpace?

Medpace offers opportunities to work in an international clinical research environment supporting pharmaceutical, biotechnology and medical-device development programs.

Employee benefits highlighted by the company include:

• Competitive compensation based on performance.
• Health, wellness, retirement and paid-time-off benefits.
• Defined career-development and advancement opportunities.
• Structured onboarding and professional training.
• Continuous learning opportunities.
• Access to experienced on-site mentors.
• Cross-functional collaboration with clinical research professionals.
• Company-sponsored social events.
• Occasional work-from-home flexibility for eligible positions after training.

Benefits can vary depending on the employee’s country and position.

How to Apply

Application Link SAS Programmer – 12315

Application Link Site Payments Processor – 12313

Application Link Experienced SAS Programmer – 12319

Application Link Regulatory Submissions Coordinator – 12919

Application Link Study Start-up Submissions Manager – 12312