Senior Research Science Liaison

Syneos Health Commercial Solutions; Hyderabad; On-site; INR 1,500,000 - 2,100,000; Full time

Job summary

Syneos Health is seeking a Senior Research Science Liaison to serve as the scientific and site-facing representative for clinical trials and medical affairs initiatives in India. You will build relationships with investigators, study coordinators, and key opinion leaders to support study execution, stakeholder engagement, and scientific exchange.

You will collaborate with clinical operations, medical monitors, and development teams to support feasibility, start-up, enrollment strategies, and

Qualifications

• Advanced degree (PhD, PharmD, MD, or equivalent) in life sciences or a related field.
• 3–5 years of relevant scientific, clinical research, medical affairs, or related experience.
• Prior field medical, Medical Science Liaison (MSL), clinical research, or medical affairs experience preferred.
• Solid understanding of the pharmaceutical, biotechnology, and clinical research environment.
• Ability to conduct scientific discussions with investigators, site personnel, and external stakeholders.
• Manage multiple priorities while delivering high-quality work in a dynamic environment.

Responsibilities

• Apply scientific and clinical knowledge to support investigator, site, and stakeholder engagement activities aligned to clinical trial and study objectives.
• Establish and maintain professional relationships with investigators, study coordinators, key opinion leaders, and other external stakeholders involved in clinical research.
• Partner with investigators, study coordinators, and clinical trial sites to support study readiness, protocol understanding, enrollment activities, and successful study conduct.
• Conduct compliant scientific engagements that support site awareness, study readiness, enrollment objectives, and clinical trial execution.
• Deliver scientific and clinical education to investigators, study coordinators, and site personnel in alignment with engagement plans, study requirements, approved materials, and protocol‑specific objectives.
• Serve as a liaison between external stakeholders and internal teams by facilitating scientific exchange, communication and follow‑up activities.
• Support feasibility, study start-up, site engagement, enrollment, and post‑activation activities across assigned programs.
• Follow up with investigators, study coordinators, and clinical trial sites to identify challenges, barriers, and opportunities that may impact enrollment, study conduct, or site performance.
• Identify site challenges, enrollment barriers, protocol implementation issues, and stakeholder feedback that may impact study execution and communicate observations and recommendations to internal teams.
• Capture, document, and communicate site insights, stakeholder feedback, field observations, and study‑related challenges to support informed decision‑making and study execution.
• Develop and maintain awareness of therapeutic area developments, clinical practice patterns, clinical strategies, and competitive landscape trends relevant to assigned programs.
• Contribute to the development and review of scientific engagement materials, educational resources, presentations, and study support materials.
• Collaborate with clinical operations, project teams, medical monitors, therapeutic area leads, recruitment and retention teams, site and patient services, and client stakeholders to support study objectives.
• Maintain accurate and timely documentation of stakeholder interactions, insights, and project activities, and provide routine updates to internal teams and clients.
• Ensure all activities are conducted in compliance with applicable regulations, industry standards, company policies, SOPs, and client requirements.
• Support additional Medical Affairs and clinical research initiatives as assigned.

Skills

Scientific communication

Stakeholder engagement

Insight generation

Site engagement

Analytical skills

Project coordination

Cross-functional collaboration

Communication

Time management

Attention to detail

Compliance

Microsoft Office

Education

Advanced degree in life sciences

Tools

Microsoft Office (PowerPoint, Excel)

Job description

Description

The Senior Research Science Liaison (Senior RSL) serves as Syneos Health's scientific and site-facing representative in support of clinical trials and medical affairs initiatives. The Senior RSL establishes and maintains professional relationships with investigators, study coordinators, clinical trial sites, key opinion leaders, and other external stakeholders to support study execution, stakeholder engagement, and scientific exchange.

The Senior RSL establishes and maintains professional relationships with investigators, study site personnel, key opinion leaders, and other external stakeholders to support clinical trial execution, site engagement, and insight generation.

Working collaboratively with clinical operations, clinical development teams, medical monitors, and other stakeholders, the Senior RSL supports feasibility activities, study start-up, site engagement, enrollment strategies, and post-activation initiatives that contribute to successful study execution.

The Senior RSL develops knowledge of therapeutic area dynamics, clinical strategies, and competitive landscape developments relevant to products under development and provides scientific observations and stakeholder feedback that help inform study teams and clients. The role operates as an individual contributor responsible for the timely, accurate, and compliant execution of assigned engagement activities and deliverables.

Job Responsibilities

• Apply scientific and clinical knowledge to support investigator, site, and stakeholder engagement activities aligned to clinical trial and study objectives.
• Establish and maintain professional relationships with investigators, study coordinators, key opinion leaders, and other external stakeholders involved in clinical research.
• Partner with investigators, study coordinators, and clinical trial sites to support study readiness, protocol understanding, enrollment activities, and successful study conduct.
• Conduct compliant scientific engagements that support site awareness, study readiness, enrollment objectives, and clinical trial execution.
• Deliver scientific and clinical education to investigators, study coordinators, and site personnel in alignment with engagement plans, study requirements, approved materials, and protocol‑specific objectives.
• Serve as a liaison between external stakeholders and internal teams by facilitating scientific exchange, communication and follow‑up activities.
• Support feasibility, study start-up, site engagement, enrollment, and post‑activation activities across assigned programs.
• Follow up with investigators, study coordinators, and clinical trial sites to identify challenges, barriers, and opportunities that may impact enrollment, study conduct, or site performance.
• Identify site challenges, enrollment barriers, protocol implementation issues, and stakeholder feedback that may impact study execution and communicate observations and recommendations to internal teams.
• Capture, document, and communicate site insights, stakeholder feedback, field observations, and study‑related challenges to support informed decision‑making and study execution.
• Develop and maintain awareness of therapeutic area developments, clinical practice patterns, clinical strategies, and competitive landscape trends relevant to assigned programs.
• Contribute to the development and review of scientific engagement materials, educational resources, presentations, and study support materials.
• Collaborate with clinical operations, project teams, medical monitors, therapeutic area leads, recruitment and retention teams, site and patient services, and client stakeholders to support study objectives.
• Maintain accurate and timely documentation of stakeholder interactions, insights, and project activities, and provide routine updates to internal teams and clients.
• Ensure all activities are conducted in compliance with applicable regulations, industry standards, company policies, SOPs, and client requirements.
• Support additional Medical Affairs and clinical research initiatives as assigned.

QUALIFICATION REQUIREMENTS (please indicate if ‘preferred’) Minimum:

• Advanced degree (PhD, PharmD, MD, or equivalent) in life sciences or a related field.
• 3–5 years of relevant scientific, clinical research, medical affairs, or related experience.

Preferred:

• Prior field medical, Medical Science Liaison (MSL), clinical research, or medical affairs experience.

Additional Qualifications

• Solid understanding of the pharmaceutical, biotechnology, and clinical research environment.
• Ability to effectively conduct scientific discussions with investigators, site personnel, and external stakeholders.
• Demonstrated ability to manage multiple priorities while delivering high‑quality work in a dynamic environment.
• Strong commitment to scientific integrity, compliance, and quality standards.

Critical Skills

• Scientific and clinical communication
• Stakeholder engagement and service orientation
• Insight generation and documentation
• Clinical trial and site engagement support
• Analytical and problem‑solving skills
• Project coordination and execution
• Cross‑functional collaboration
• Written and verbal communication
• Organization and time management
• Attention to detail and quality
• Compliance and professional judgment
• Proficiency in Microsoft Office, including PowerPoint and Excel

At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. If your past experience doesn’t align perfectly, we encourage you to apply anyway. At times, we will consider transferable skills from previous roles. We also encourage you to join our Talent Network to stay connected to additional career opportunities.

Why Syneos Health?

Here, you’re a part of the big picture. You will collaborate with colleagues across clinical and commercial disciplines to guide premarket development through post‑market commercial strategy. Every project is a chance to solve a new challenge, learn from your colleagues, and advance your career. The diversification and breadth of our new and existing partnerships create a multitude of career paths and employment opportunities. Join our game‑changing, global company dedicated to creating better, smarter, faster ways to get biopharmaceutical therapies to patients. Experience the thrill of knowing that your everyday efforts are contributing to improving patients’ lives around the world.

Work Here Matters Everywhere | How are you inspired to change lives?

Syneos Health companies are affirmative action/equal opportunity employers (Minorities/Females/Veterans/Disabled)