Apply for Clinical Research Associate (CRA) role at Catalyst

Stelis Biopharma Ltd; New Delhi; On-site; INR 900,000 - 1,300,000; Full time

Job summary

Catalyst Clinical Services in Delhi is seeking a Clinical Research Associate (CRA) with M.Pharm or Ph.D and 2+ years of on-site monitoring experience to join our expanding team. You will conduct on-site monitoring, ensure GCP compliance, and support investigators to execute trials smoothly.

This role focuses on data review, site issue resolution, and patient safety, with responsibilities across regulatory adherence, SOPs, and multi-site coordination.

Qualifications

• M.Pharm or Ph.D in Oncology, Diabetes, Medical Devices, or related areas.
• At least 2 years of on-site clinical trial monitoring experience.
• Strong knowledge of GCP guidelines and regulatory requirements.

Responsibilities

• Conducting on-site monitoring of clinical trials.
• Ensuring adherence to Good Clinical Practice (GCP), regulatory guidelines, and company SOPs.
• Supporting investigators and site staff in smooth trial execution.
• Reviewing trial data for accuracy, consistency, and completeness.
• Preparing monitoring visit reports and ensuring timely resolution of site issues.
• Maintaining patient safety and compliance with ethical standards.

Skills

GCP knowledge

Excellent communication

Site management

Ethical research

Education

M.Pharm

Ph.D

Job description

M.Pharm/Ph.D Clinical Research Associate Vacancy in Delhi

Apply for Clinical Research Associate (CRA) role at Catalyst in Delhi. Openings for M.Pharm/Ph.D with 2+ years of on-site monitoring experience.

At Catalyst Clinical Services, we are expanding our team and inviting skilled professionals to join us as Clinical Research Associates (CRA) in Delhi. This is a rewarding opportunity for those passionate about clinical trials, regulatory compliance, and advancing patient-centric healthcare research.

Company Overview

Catalyst Clinical Services is a trusted name in clinical research, dedicated to improving healthcare outcomes through high-quality, ethical, and innovative clinical trials. With expertise across multiple therapeutic areas such as oncology, diabetes, and medical devices, Catalyst fosters an environment where professionals can thrive and contribute to meaningful scientific advancements.

Job Role & Responsibilities

As a Clinical Research Associate (CRA), you will be responsible for:

• Conducting on-site monitoring of clinical trials.
• Ensuring adherence to Good Clinical Practice (GCP), regulatory guidelines, and company SOPs.
• Supporting investigators and site staff in smooth trial execution.
• Reviewing trial data for accuracy, consistency, and completeness.
• Preparing monitoring visit reports and ensuring timely resolution of site issues.
• Maintaining patient safety and compliance with ethical standards.

Eligibility / Qualifications

• Education: M.Pharm, Ph.D (Oncology, Diabetes, Medical Devices, or related areas).
• Experience: Minimum 2 years of on-site clinical trial monitoring experience.
• Skills:
  • Strong knowledge of GCP guidelines and regulatory requirements.
  • Excellent communication and interpersonal skills.
  • Ability to manage multiple clinical trial sites effectively.
  • Commitment to patient-centric and ethical research practices.

Location & Salary

• Job Location: Delhi, India
• Salary: Competitive package aligned with industry standards and candidate expertise.

FAQs

Q1: Who can apply for the CRA role at Catalyst?
Candidates with an M.Pharm or Ph.D. and at least 2 years of on-site clinical trial monitoring experience can apply.

Q2: What therapeutic areas are preferred?
Expertise in oncology, diabetes, or medical devices is preferred but not mandatory.

Q3: Where is the job located?
The CRA position is based in Delhi, India.

Q5: Is previous CRA experience mandatory?
Yes, a minimum of 2 years of on-site monitoring experience is required.