Insignia Hiring Clinical Research Associates

Postgrad Clinical Research Associate Openings | Delhi

Insignia hiring 5 Clinical Research Associates (Postgrad, 3+ yrs, onsite Delhi). Apply for CRA monitoring roles now.

Insignia Clinical Services is hiring experienced Clinical Research Associates (CRAs) to join its monitoring team at the NSP Delhi office. These are full-time onsite positions for candidates with hands-on clinical trial monitoring experience who are ready to relocate to Delhi and take ownership of trial site quality, data integrity and regulatory compliance.

Insignia seeks driven life-science postgraduates who can manage study initiation, perform site monitoring, maintain regulatory compliance and contribute to high-quality clinical trial delivery. If you’re looking for a role that blends field monitoring with data oversight and cross-functional collaboration, this opening offers steady career growth in clinical operations.

Company Overview

Insignia Clinical Services is a clinical research organisation that delivers end-to-end clinical trial support across phases I–IV. The company focuses on quality-driven clinical monitoring, regulatory compliance (ICH-GCP), and timely study execution for sponsors across therapeutic areas. Insignia’s teams work closely with sites, investigators, and sponsors to ensure participant safety and data reliability—critical factors that keep investigational medicines on track for approval and patient access.

Job Role & Responsibilities

Position: Clinical Research Associate (CRA)
No. of Positions: 5
Work Mode: Full-time, Onsite (NSP, Delhi)
Relocation: Candidates must be willing to relocate to Delhi

Primary Responsibilities

• Study initiation: prepare site packets, conduct initiation visits, and ensure sites are study-ready.
• Monitoring and site management: conduct routine monitoring visits, source-data verification (SDV), and ensure protocol adherence.
• Compliance and quality assurance: verify regulatory binders, informed consent, SAE reporting, and adherence to ICH‑GCP norms.
• Communication and reporting: prepare monitoring visit reports, highlight action items, and follow up on CAPA and open queries.
• Data management: collaborate with data managers for query resolution and ensure data integrity during transfers.
• Risk management: identify site-level risks, escalate issues, and implement monitoring plans to mitigate them.

What success looks like

• High-quality monitoring reports with clear, actionable findings.
• Reduced query turnaround time and improved site compliance metrics.
• Smooth study initiations and on-time milestone achievement.

Eligibility / Qualifications

Essential qualification: Postgraduate degree in Life Sciences, Pharmacy, Nursing, or related field.
Experience: Minimum 3 years in clinical research, including at least one year of onsite monitoring in clinical trials.

Relevant courses and certifications (comma-separated): M.Sc Life Sciences, M.Pharm, Clinical Research Certification, ICH-GCP Training, Monitoring Workshop, Pharmacovigilance Basics.

Required skills

• Strong working knowledge of ICH‑GCP, regulatory requirements, and trial documentation.
• Proven experience in site monitoring, SDV, SAE handling, and regulatory binder maintenance.
• Excellent written and verbal communication skills for reporting and site interactions.
• Familiarity with EDC systems and clinical data capture workflows.
• Strong organizational skills and ability to work independently on multiple studies.

Location & Salary

Location: NSP, Delhi (onsite) — candidates must be ready to relocate.
Salary: Competitive — offered as per industry norms and experience. Exact CTC will be discussed during the interview.

Application Process

Email your CV to careers@insigniacs.com with subject line: Application for CRA position – [Your Name].

Please include:

• Updated resume with clinical trial experience and onsite monitoring details.
• List of therapeutic areas and study phases handled.
• Notice period, current CTC, and expected salary.

Shortlisted candidates will be contacted for a telephonic screening followed by technical and HR interviews.

FAQs

Q1. Is relocation support provided?
A1. Relocation discussions will be handled at the time of offer depending on seniority and business needs.

Q2. Are remote or hybrid options available?
A2. These positions are full-time onsite at the NSP Delhi office; remote work is not available.

Q3. What therapeutic areas will I work in?
A3. Insignia works across multiple therapeutic areas and phases; details will be shared during interviews based on project needs.

Q4. Do I need EDC experience?
A4. Familiarity with EDC and clinical data capture systems is preferred; training will be provided for the company’s specific platforms.

Q5. What does the selection process involve?
A5. Telephonic screening → Technical interview (clinical monitoring focus) → HR interview and offer.

Summary Table

Company	Insignia Clinical Services
Vacancies	5 Clinical Research Associates (Onsite)
Required Education	Postgraduate in Life Sciences, Pharmacy, Nursing or related fields
Experience	Minimum 3 years in clinical research with at least 1 year onsite monitoring