Syneos Health Hiring CRA – Future Roles in Gurugram | PharmaHiringHub

Syneos health; Gurugram District; Vor Ort; INR 600.000 - 800.000; Vollzeit

Benefits dieser Stelle

Exposure to global clinical research projects

Career development programs

Training in advanced areas

Competitive salary

Opportunities for innovative projects

Zusammenfassung

Syneos Health is hiring for a Clinical Research Associate (CRA) position based in Gurugram, India, with a hybrid work model. This role offers global exposure and is ideal for candidates experienced in clinical trial monitoring.

The CRA will manage clinical trial activities and collaborate with teams to ensure regulatory compliance. Candidates should have a Bachelor’s degree in Life Sciences or related fields and be willing to travel up to 75% of the time.

Qualifikationen

• Bachelor’s degree in a relevant field.
• Good understanding of ICH-GCP guidelines.
• Experience in clinical trial monitoring and site management.
• Ability to handle documentation tasks.
• Willingness to travel up to 75%.

Aufgaben

• Managing clinical trial activities according to regulatory guidelines.
• Conducting site qualifications and monitoring visits.
• Ensuring compliance with ICH-GCP guidelines.

Kenntnisse

Clinical trial monitoring

Regulatory compliance

Strong communication skills

Interpersonal skills

EDC systems familiarity

Ausbildung

Bachelor's degree in Life Sciences, Pharmacy, Nursing

Jobbeschreibung

If you are looking for jobs in clinical research, this opportunity from Syneos Health could be the right fit. The company is hiring for Clinical Research Associate (CRA) – Future Roles (India) based in Gurugram with a hybrid work model.

CRA roles continue to be in high demand across India as global CROs expand into areas like oncology, pharmacovigilance, vaccines, and clinical development programs. For professionals with experience in clinical monitoring and trial operations, this role offers both growth and international exposure.

About organization

Syneos Health is a leading global Contract Research Organization (CRO) that supports pharmaceutical and biotechnology companies in developing and delivering new treatments.

The company works across a wide range of clinical and commercial services, including:

• Regulatory support
• Medical affairs
• Real-world evidence studies

Syneos Health has contributed significantly to drug development worldwide, supporting a large percentage of FDA and EMA-approved drugs in recent years. Working here gives you exposure to global clinical research standards and large-scale studies.

Role Overview

Here’s a quick summary of the role:

• Role: Clinical Research Associate (CRA) – Future Roles (India)
• Location: Gurugram
• Work Mode: Hybrid
• Job Type: Full-Time
• Department: Clinical Research
• Requisition ID: 25106957

This role is ideal for candidates who already have some experience in clinical trial monitoring, site management, and regulatory compliance.

Key Responsibilities of a CRA

As a Clinical Research Associate, your role will involve managing clinical trial activities and ensuring that studies are conducted according to regulatory guidelines.

Core Responsibilities:

• Conducting site qualification, initiation, monitoring, and close-out visits
• Ensuring compliance with ICH-GCP guidelines, protocols, and SOPs
• Performing Source Document Review (SDR) and verifying CRF data
• Monitoring patient safety, informed consent, and ethical compliance
• Resolving data queries within project timelines
• Maintaining and reviewing Investigator Site Files (ISF)
• Ensuring reconciliation with the Trial Master File (TMF)
• Checking investigational product (IP) accountability and storage
• Supporting patient recruitment and retention strategies
• Managing travel-based monitoring visits across India

Additional Responsibilities (Real-World Studies)

For Real World Late Phase (RWLP) projects, you may also work on:

• Chart abstraction and real-world data collection
• Supporting real-world evidence (RWE) studies
• Collaborating with medical and sponsor teams
• Managing complete site lifecycle from startup to closure

This adds another layer of learning, especially for those interested in healthcare analytics and real-world data.

Qualifications Needed

To apply for this role, candidates should meet the following criteria:

Educational Qualification:

• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field
• Registered Nurse (RN) candidates may also be considered

• Good understanding of ICH-GCP guidelines and regulatory requirements
• Experience in clinical trial monitoring and site management
• Strong communication and interpersonal skills
• Familiarity with EDC systems and clinical tools
• Ability to handle documentation and reporting tasks
• Willingness to travel up to 75%

This role is best suited for candidates who are comfortable with fieldwork and site visits.

Why Consider a CRA Role at Syneos Health?

Clinical Research Associate roles are considered one of the most promising career paths in the life sciences industry. This opportunity offers several advantages.

1. Global Exposure

You’ll work on international clinical trials and interact with global teams and sponsors.

2. Hybrid Work Model

The flexibility of hybrid work helps maintain a better work-life balance while still gaining on-site experience.

CRA roles often lead to positions such as:

• Senior CRA
• Lead CRA
• Clinical Trial Manager (CTM)
• Project Manager

4. Diverse Therapeutic Areas

You may get exposure to areas like oncology, vaccines, rare diseases, and medical affairs.

Benefits of Working with Syneos Health

Syneos Health provides a well-structured work environment along with several professional benefits:

• Exposure to global clinical research projects
• Career development and internal growth programs
• Training in advanced clinical and therapeutic areas
• Competitive salary and rewards
• Opportunities to work on innovative drug development programs

For professionals looking to grow in clinical research, this environment can be very rewarding.

Job Location & Work Model

Gurugram (Hybrid Role)

The hybrid model allows you to split your time between office work, remote tasks, and on-site monitoring visits. Since CRA roles involve site monitoring, candidates should be comfortable with travel.

Who Should Apply?

This role is best suited for:

• Professionals with experience in clinical trial monitoring
• Candidates familiar with ICH-GCP guidelines
• Individuals interested in long-term careers in clinical research
• Those willing to travel and work in dynamic environments

If you already have some exposure to clinical operations or pharmacovigilance, this role can help you level up your career.

These positions are part of Syneos Health’s Talent Pipeline, created to identify and pre‑screen candidates for CRA openings. By applying, candidates will be considered for future hiring needs and contacted when relevant opportunities become available.

How to Apply

Interested candidates can apply through the official Syneos health careers page:

It is recommended to apply as early as possible, since roles for freshers often receive a high number of applications.