Chisquare Labs – Hiring for Clinical and Regulatory Roles

Chisquare Labs, a leader in clinical research and regulatory solutions, is excited to announce multiple job openings for motivated professionals. We are hiring for Clinical Case Processing Associate, Clinical Research Data Analyst, and Global Regulatory Specialist roles to support our mission of advancing healthcare innovation.

Whether you’re experienced in pharmacovigilance, clinical research, or regulatory affairs, we invite you to join our team in full-time or part-time capacities, with remote and hybrid options available!

About Chisquare Labs

Chisquare Labs is dedicated to delivering high-quality clinical research, safety case management, and regulatory services. We are seeking talented individuals with backgrounds in life sciences, pharmacy, and related fields to contribute to our growing operations. Join us to make an impact in a dynamic and collaborative environment.

Job Opportunities

We are hiring for the following positions:

Clinical Case Processing Associate

  • Job Type: Full-Time, Remote
  • Qualification: Degree in Life Sciences, Pharm D, M.Pharm, or a related field
  • Experience: 1-2 years in Pharmacovigilance, Clinical Research, Safety Case Management, or a related role (preferred)
  • Description: Support the processing and management of clinical safety cases, ensuring compliance with regulatory standards and contributing to patient safety initiatives.

Clinical Research Data Analyst

  • Job Type: Full-Time, Hybrid
  • Qualification: Pharm D, M.Pharm, or a related field
  • Experience: 6 months to 1 year in CRO, Clinical Pharmacy, Medical Coding, or Scientific Writing
  • Description: Analyze clinical research data to support study outcomes, leveraging your skills in a hybrid work setting that combines remote and on-site collaboration.

Global Regulatory Specialist

  • Job Type: Full-Time or Part-Time, Remote
  • Qualification:
    • Bachelor’s degree in Pharm D, Medicine, or a related field, OR
    • Master’s degree in Regulatory Affairs or M.Pharm
  • Experience: 3-4 years in Global Regulatory Submissions
  • Description: Lead and support global regulatory submissions, ensuring compliance with international standards and facilitating the approval of innovative healthcare products.
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How to Apply

Interested candidates can apply by:

  • Sending their resume to the official Chisquare Labs HR email (not provided in the original posting—please check the company website or contact HR for details).
  • Including the job title (e.g., “Clinical Case Processing Associate”) in the subject line of your application email.
Chisquare Labs – Hiring for Clinical and Regulatory Roles
Chisquare Labs – Hiring for Clinical and Regulatory Roles
Chisquare Labs – Hiring for Clinical and Regulatory Roles

For more information or to confirm the application process, visit our website (URL not provided—please refer to Chisquare Labs’ official site).

Why Join Chisquare Labs?

Chisquare Labs offers a flexible and innovative workplace where you can grow your career in clinical research and regulatory affairs. With remote and hybrid options, we prioritize work-life balance while delivering impactful solutions in the life sciences industry.

Take the Next Step

Apply today to join our team and contribute to advancing healthcare globally. We look forward to welcoming passionate professionals to Chisquare Labs!

Chisquare Labs is an equal-opportunity employer committed to diversity and inclusion.

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