Insignia Clinical Services (ICS) is a premier Indian Contract Research Organization (CRO) headquartered in New Delhi, founded in 2010. With 51-200 employees and a focus on pharmaceutical manufacturing, biotechnology, medical devices, and more, ICS delivers end-to-end solutions for clinical trials (Phase I-IV), regulatory affairs, non-clinical studies, medical writing, and pharmacovigilance. Servicing clients in pharmaceuticals, cosmetics, food supplements, and agrochemicals, the company stands out for its innovative, scalable services—from regulatory strategy and submission to patient recruitment and data management.
What sets Insignia apart in the competitive CRO landscape in India? Their commitment to excellence, timely project management, and ancillary services like government liaisoning, distributor qualification, and regulatory intelligence. As a privately held firm, ICS empowers multinational companies, Indian manufacturers, and importers to navigate product lifecycles from concept to commercialization. With specialties in biostatistics, clinical data management, EDC tools, and real-world clinical trials, Insignia is at the forefront of healthcare innovation.
Recent highlights include their 13th anniversary celebrations, emphasizing team growth and leadership training, and active hiring drives for clinical research jobs. Follow them on LinkedIn (9,590+ followers) or visit www.insigniacs.com for more on their mission: “Simplified Solutions Driven Towards Excellence.” If you’re seeking stable clinical trials jobs in Delhi, Insignia offers a collaborative culture with opportunities in a 5,12,000 sq ft office at Best Sky Tower, NSP, Delhi.
(Suggested Image: Company headquarters in Pitampura, Delhi. Alt-text: “Insignia Clinical Services office for CRO jobs Delhi”.)
Job Description: Senior Executive – Clinical Data Management
Insignia Clinical Services is seeking talented individuals for 2 vacancies in Senior Executive – Clinical Data Management. This role is pivotal in managing clinical study data to support groundbreaking pharmaceutical research. Ideal for those with a background in life sciences, you’ll ensure data integrity, compliance, and efficiency in clinical trials.
Key Responsibilities:
- Manage clinical study documents, including database setup and Case Report Form (CRF) completion.
- Perform accurate data entry, query handling, and resolution to maintain database cleanliness.
- Ensure high data quality and adherence to regulatory standards like GCP, ICH guidelines, and 21 CFR Part 11.
- Assist with user training, access management, and database lock processes.
- Deliver high-quality, analysis-ready datasets for statistical programming and reporting.
- Collaborate on site feasibility assessments, budget management, and site initiation for seamless trial operations.
- Support electronic data capture (EDC) tools and clinical trial management systems (CTMS) for efficient workflows.
This office-based, full-time position in NSP, Delhi, requires candidates to be ready to relocate. It’s perfect for professionals driving clinical data management in fast-paced CRO environments.
Qualifications and Experience:
- Experience: Minimum 3+ years in Clinical Data Management, preferably in a CRO or pharma setting.
- Education: Master’s in Life Sciences, B.Pharma, or related degrees/diplomas.
- Skills:
- Strong knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH), and regulatory guidelines.
- Proficiency in CTMS, CRF design, EDC tools (e.g., Medidata Rave, Oracle Clinical), and data validation techniques.
- Excellent organizational, communication, and interpersonal skills for team collaboration.
- Ability to work independently while contributing to cross-functional teams.
- Bonus: Experience in site feasibility, budget oversight, and project timelines for clinical trials jobs.
Salary and Benefits:
- Salary: Competitive, as per industry norms (typically ₹6-10 LPA for mid-level roles, based on experience).
- Location: Netaji Subhash Place (NSP), Pitampura, New Delhi 110034 (Relocation support may be discussed).
- Perks: Dynamic team environment, professional growth opportunities, and exposure to global pharma projects.
If you thrive in clinical research jobs and want to advance your career in data management for clinical trials, this role at Insignia is a game-changer.
(Suggested Internal Link: Explore more CRO jobs in Delhi on Pharmabharat.org.)
How to Apply for Senior Executive – Clinical Data Management at Insignia
Ready to take the next step in your clinical data management career? Applying is simple and straightforward:
- Prepare Your CV: Highlight your 3+ years in clinical data management, EDC proficiency, and relevant clinical trials experience.
- Email Your Application: Send your updated CV to careers@insigniacs.com.
- Subject Line: Use “Sr. Executive – Clinical Data Management” or “Application for Sr. Exec – Clinical Data Management” for quick processing.
- What to Include: Cover letter mentioning why you’re excited about Insignia Clinical Services hiring and your fit for CRO jobs in Delhi. Note your willingness to relocate to Delhi.
- Timeline: Applications are open now—apply ASAP as spots are limited to 2 vacancies. Shortlisted candidates will be contacted for interviews within 1-2 weeks.
For queries, visit www.insigniacs.com or connect on LinkedIn. Join thousands of pharma professionals finding opportunities on Pharmabharat.org—your go-to site for pharma jobs in India!
