Are you a pharmacy or life sciences professional looking for a rewarding career in the pharmaceutical and clinical research industry? Chisquare Labs is hiring for multiple positions, including Clinical Research Data Analyst, Clinical Case Processing Associate, and Global Regulatory Specialist. These roles offer a mix of full-time, hybrid, and remote opportunities, making them ideal for candidates seeking flexibility and growth in their careers. Read on to learn more about these exciting job openings and how you can apply!
Clinical Research Data Analyst
Qualifications:
- Pharm D, M Pharm, or a related degree.
- 6 months to 1 year of experience in fields such as CRO (Contract Research Organization), Clinical Pharmacy, Medical Coding, or Scientific Writing.
Role Overview:
As a Clinical Research Data Analyst, you will play a crucial role in analyzing and interpreting clinical trial data. Your responsibilities will include ensuring data accuracy, preparing reports, and collaborating with cross-functional teams to support research objectives. This hybrid role offers the perfect balance of in-office collaboration and remote work flexibility.
Clinical Case Processing Associate
Qualifications:
- Life Sciences, Pharm D, or M Pharm degree.
- 1-2 years of experience in Pharmacovigilance, Clinical Research, Safety Case Management, or a related field (preferred).
Role Overview:
The Clinical Case Processing Associate will be responsible for managing and processing safety data, ensuring compliance with regulatory standards, and maintaining accurate documentation. This fully remote position is ideal for professionals who thrive in independent work environments and have a strong attention to detail.
Global Regulatory Specialist
Qualifications:
- Bachelor’s degree in Pharm D, Medicine, or a related field.
- OR a Master’s degree in Regulatory Affairs or M Pharm.
- 3-4 years of experience in Global Regulatory Submissions.
Role Overview:
As a Global Regulatory Specialist, you will be responsible for preparing and submitting regulatory documents to global health authorities. Your expertise will ensure compliance with international regulations and support the successful approval of pharmaceutical products. This role offers the flexibility of full-time or part-time remote work, making it suitable for experienced professionals seeking work-life balance.
Interested in joining our team? Send your resume to careers@chisquarelabs.com with the job title in the subject line!
