Insignia Clinical Services Hiring for Senior Executive – Project Management in Delhi

Are you ready to become a future clinical research leader in the dynamic field of clinical trials? Insignia Clinical Services Limited, a leading Indian Contract Research Organization (CRO) headquartered in New Delhi, is hiring Senior Executives for Project Management within our Clinical Operations Team.

With a vision of delivering Simplified Solutions Driven Towards Excellence, Insignia supports global pharmaceutical, biotechnology, and medical device industries through innovative clinical research services. Join our team to drive high-impact clinical trials and advance your career in clinical research management.

Application Details

Notes:

  • Candidates must submit an updated CV, academic certificates, experience letters, and recent payslips.
  • Immediate joiners are preferred.
  • Salary is competitive and aligned with industry norms.

Why Join Insignia Clinical Services?

Founded in 2012, Insignia Clinical Services (ICS) is a trusted CRO providing end-to-end clinical research solutions, from regulatory affairs to clinical trial management and pharmacovigilance. With over 80 employees and a 3.2/5 rating on AmbitionBox for supportive work culture, ICS is recognized for its commitment to quality and innovation.

Our New Delhi headquarters fosters collaboration, offering opportunities to work on Phase I-IV clinical trials for global clients in pharmaceuticals, biotech, and medical devices. Join us to shape the future of clinical research with a team of seasoned experts.

Job Position: Senior Executive – Project Management (Clinical Operations)

We are seeking three experienced professionals to lead project management in our Clinical Operations Team, ensuring the success of clinical trials through strategic oversight and compliance.

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Job Details

  • Experience: 3+ years as a Clinical Research Professional
  • Qualification: Master’s in Life Sciences, B.Pharma, or related degrees/diploma
  • Location: New Delhi, Delhi (Office-based)
  • Department: Clinical Operations
  • Vacancies: 3

Key Responsibilities

Clinical Trial Project Management

  • Oversee end-to-end management of clinical trials (Phase I-IV), ensuring timely execution and compliance with GCP guidelines
  • Develop and manage project timelines, budgets, and resource allocation for clinical studies
  • Coordinate with cross-functional teams, including data management, biostatistics, and medical writing

Site and Stakeholder Coordination

  • Facilitate site selection, investigator recruitment, and patient enrollment to meet trial objectives
  • Liaise with clinical sites, sponsors, and regulatory authorities to ensure seamless operations
  • Monitor site performance and patient engagement to optimize trial outcomes

Quality and Compliance

  • Ensure adherence to regulatory requirements, including ICH-GCP, FDA, and CDSCO guidelines
  • Conduct risk assessments and implement mitigation strategies to maintain trial integrity
  • Support quality assurance audits and ensure compliance with SOPs and protocols

Reporting and Communication

  • Prepare and deliver project status reports to stakeholders and sponsors
  • Maintain clear and effective communication with internal teams and external partners
  • Document trial progress and ensure accurate data reporting for regulatory submissions

Required Skills and Qualifications

CategoryDetails
EducationMaster’s in Life Sciences, B.Pharma, or related degrees/diploma
Experience3+ years in clinical research, preferably in a CRO or pharmaceutical setting
Technical SkillsKnowledge of clinical trial protocols, GCP, and regulatory guidelines
Soft SkillsExcellent communication, leadership, and project management skills
Preferred ExpertiseExperience in site monitoring, patient recruitment, or team leadership
ToolsFamiliarity with CTMS, EDC systems, and MS Office (Excel, PowerPoint)

Why This Role?

  • Leadership Opportunities: Lead high-impact clinical trials and grow into a clinical research leader.
  • Global Exposure: Work with international pharmaceutical and biotech clients on cutting-edge studies.
  • Competitive Salary: Earn a salary aligned with industry standards (₹4–5 Lakhs per annum for similar roles, per AmbitionBox).
  • Innovative Environment: Join a CRO known for its proactive approach to trial optimization and regulatory compliance.
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How to Apply

To apply for the Senior Executive – Project Management position, follow these steps:

  • Prepare Your Documents: Update your CV, highlighting your 3+ years of clinical research experience, and gather academic certificates (Master’s/B.Pharma), experience letters, and payslips.
  • Email Your Application: Send your documents to careers@insigniacs.com with the subject line “Senior Executive Project Management – Delhi.”
  • Include Key Details: Mention your total experience, current CTC, expected CTC, and notice period.
  • Research Insignia: Visit www.insigniacs.com and LinkedIn to learn about our clinical trial expertise and innovative solutions.
  • Prepare for the Interview: Be ready to discuss your experience with clinical trial management, GCP compliance, or site coordination.
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Insignia Clinical Services Hiring for Senior Executive – Project Management in Delhi

Why Delhi?

New Delhi, India’s capital, is a hub for clinical research and healthcare innovation, offering unmatched career opportunities. Insignia’s office in Pitampura, located at 512, Best Sky Tower, Netaji Subhash Place, is well-connected and equipped with modern facilities, fostering a collaborative work environment. Learn more about Delhi’s healthcare ecosystem.

Contact Information

For inquiries or to apply, reach out to:

Don’t miss this chance to join a leading CRO and advance your career in clinical research. Apply by May 15, 2025, and become a future clinical leader with Insignia Clinical Services!

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