Join Chisquare Labs – Exciting Career Opportunities Await!

Chisquare Labs is growing, and we are actively looking for talented professionals to join our dynamic team. If you have a passion for clinical research, regulatory affairs, and data analysis, this is your opportunity to contribute to cutting-edge projects while advancing your career. We offer remote, hybrid, and full-time positions with competitive compensation and growth opportunities.

Open Positions

1. Clinical Case Processing Associate

Job Type: Full-Time | Remote

Qualifications:

A Bachelor’s or Master’s degree in Life Sciences, Pharm D, M Pharm, or a related field.
Strong knowledge of clinical safety, pharmacovigilance, and case processing.

Experience:

1–2 years of experience in Pharmacovigilance, Clinical Research, Drug Safety, or Case Management (preferred).
Familiarity with MedDRA coding, ICSR (Individual Case Safety Reports), and regulatory compliance.
Understanding of Good Pharmacovigilance Practices (GVP).

Key Responsibilities:

Assessing and processing adverse event reports for pharmaceutical and biotech companies.
Ensuring compliance with FDA, EMA, and MHRA regulations.
Using safety databases to manage case processing activities.
Collaborating with cross-functional teams to ensure data accuracy.

2. Global Regulatory Specialist

Job Type: Full-Time/Part-Time | Remote

Qualifications:

A Bachelor’s degree in Pharm D, Medicine, or a related field.
OR a Master’s degree in Regulatory Affairs, M Pharm.

Experience:

3–4 years of experience in Global Regulatory Affairs with a focus on regulatory submissions.
Strong knowledge of ICH, FDA, EMA, and WHO regulatory requirements.
Experience with eCTD (electronic Common Technical Document) submissions.

Key Responsibilities:

Preparing and submitting global regulatory documents for new drug applications.
Managing and compiling regulatory dossiers in compliance with international guidelines.
Liaising with regulatory agencies to ensure timely approvals.
Keeping track of regulatory updates and amendments to ensure adherence.

3. Clinical Research Data Analyst

Job Type: Full-Time | Hybrid

Qualifications:

A Bachelor’s or Master’s degree in Pharm D, M Pharm, or a related field.
Strong knowledge of clinical research methodologies and biostatistics.

Experience:

6 months to 1 year of experience in any of the following areas:
- CRO (Contract Research Organization) operations
- Clinical Data Management & Analysis
- Medical Coding & Scientific Writing

Key Responsibilities:

Analyzing clinical trial data for safety and efficacy trends.
Preparing reports and statistical analyses for research studies.
Ensuring compliance with GCP (Good Clinical Practice) guidelines.
Collaborating with medical writers, statisticians, and regulatory teams.

Why Join Chisquare Labs?

Competitive Salary & Benefits: We offer industry-leading compensation and benefits packages.
Remote Work Flexibility: Work from anywhere with a supportive, collaborative team.
Career Growth & Learning: We invest in your professional development with training programs and growth opportunities.
Cutting-Edge Research: Be part of innovative clinical research and regulatory projects.