WhatsApp Group Join Now
Telegram Group Join Now

Clinical Research Associate CRA Job in Delhi at Catalyst Clinical Services

Clinical Research Associate CRA Job in Delhi at Catalyst Clinical Services. Apply via email for CRA role with 2 years experience in monitoring.

Professionals with experience in clinical trials and site monitoring now have an excellent opportunity to advance their careers in clinical research. A growing clinical research organization is hiring Clinical Research Associates (CRA) for Delhi. This role is ideal for candidates with hands-on monitoring experience and strong knowledge of regulatory compliance and ICH-GCP guidelines.


Company Overview

Catalyst Clinical Services is a clinical research organization focused on delivering high-quality clinical trial services. The company supports pharmaceutical and biotech organizations with monitoring, regulatory compliance, and clinical operations. With a strong emphasis on quality and innovation, Catalyst provides professionals an opportunity to work on impactful clinical research projects.


Job Overview (Job Details)

CategoryDetails
OrganizationCatalyst Clinical Services
RoleClinical Research Associate (CRA)
QualificationBachelor’s / Master’s in Life Sciences / Pharmacy
Experience2 Years
Job LocationDelhi
Employment TypeFull-Time
Application ModeEmail
Salary₹6,00,000 – ₹10,00,000 per annum (Approx.)

Job Location & Employment Type

The role is based in Delhi and involves frequent travel for on-site monitoring visits. This is a full-time opportunity in clinical operations.


Open Positions / Department Details

The hiring is for the Clinical Operations department, where candidates will work as Clinical Research Associates managing clinical trial sites and ensuring regulatory compliance.


Key Roles & Responsibilities

Selected candidates will be responsible for:

  • Conducting site monitoring visits such as SIV (Site Initiation Visit), IMV (Interim Monitoring Visit), and COV (Close-Out Visit)
  • Ensuring compliance with ICH-GCP guidelines and regulatory standards
  • Reviewing site data for accuracy, completeness, and protocol adherence
  • Identifying deviations and escalating quality issues
  • Coordinating with investigators, site staff, and sponsors
  • Managing clinical trial documentation and audit readiness
  • Ensuring timelines and deliverables are met across assigned sites
Related Jobs  Micro Data Labs Hiring Clinical Research Coordinator Jobs Apply Now

Eligibility Criteria

Education

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

Experience

  • Minimum 2 years of on-site monitoring experience
    OR
  • 50+ monitoring visits

Skills Required

  • Strong understanding of ICH-GCP and regulatory requirements
  • Knowledge of clinical trial processes and site management
  • Excellent communication and coordination skills
  • Problem-solving and analytical ability
  • Willingness to travel frequently

Preferred Skills

  • Experience in multi-center clinical trials
  • Knowledge of TMF / eTMF systems
  • Exposure to audit and inspection readiness
  • Ability to manage multiple sites simultaneously

Salary & Benefits

  • Estimated salary: ₹6 LPA – ₹10 LPA
  • Opportunity to work on global clinical trials
  • Career growth in clinical operations
  • Exposure to regulatory compliance and monitoring excellence
  • Continuous learning and professional development

Selection Process

The hiring process typically includes:

  1. Resume Screening
  2. Technical Interview (Clinical Operations & GCP)
  3. HR Discussion
  4. Final Selection

How to Apply

Interested candidates can apply by sending their updated resume to:

Ensure your CV highlights your monitoring experience and clinical trial exposure.


Important Dates

  • Last Date to Apply: Not specified

Why Apply for This Pharma Job?

This role provides an excellent opportunity to work on end-to-end clinical trials and gain hands-on experience in monitoring and regulatory compliance. Clinical Research Associates play a crucial role in ensuring trial quality and patient safety.

With increasing demand for skilled CRAs in India and globally, this role offers strong career growth, international exposure, and long-term opportunities in clinical research.


Important Note / Disclaimer

IndiaPharmaJobs.in is an independent job information platform and is not affiliated with any recruiter or company. We do not charge any fee for job applications. Candidates are advised to verify all details independently before applying.

Related Jobs  IRT Coordinator Remote Job at Alimentiv

Final Call-to-Action

If you have experience in clinical monitoring and want to grow in clinical research, this is the right opportunity. Apply now and take the next step in your CRA career.


WhatsApp Group Join Now
Telegram Group Join Now

Leave a Comment

Join WhatsApp
Join Telegram
Telegram
DMCA.com Protection Status
Submit Resume