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ClinChoice

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The Standard of Excellence

Horsham, Pennsylvania

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Pharmaceutical Manufacturing
1,001–5,000 people

About

ClinChoice is a leading global full & functional service CRO, renowned for its exceptional product development and lifecycle management capabilities across the pharmaceutical, biotechnology, medical device, and consumer health sectors. With three decades of proven expertise and outstanding results, we excel in delivering top-tier services. Our deep regulatory expertise, clinical trial execution, and robust pharmacovigilance and biometrics capabilities position us as a trusted partner in global markets. ClinChoice proudly maintains a strong presence across the Americas, Europe, and Asia-Pacific, ensuring comprehensive support for our clients worldwide.

Open positions

Associate, Regulatory Affairs Consultant

On-site

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice is searching for a Formula/Product Compliance Associate Consultant with HYBRID option in CANADA for 12 months CONTRACT , to join one of our major consumer products clients. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. We are currently seeking a Formula/Product Compliance Associate Consultant to s…

Sr. RA Associate Consultant

Remote · Canada

The Regulatory Affairs Associate will collaborate with project teams to create and update technical documentation in compliance with EU MDR and global regulatory requirements. Responsibilities include performing quality control checks, managing regulatory submissions, and acting as a liaison between cross-functional teams and local affiliates.

Data Manager-Permanent_Hybrid@Ontario,Canada

Hybrid · Mississauga

The Data Manager is responsible for leading clinical trial data management activities, including database setup, study conduct, and close-out. They will collaborate with cross-functional teams to ensure high-quality deliverables and adherence to project timelines.

Senior Statistical Programmer Analyst - Permanent Role_Canada

Remote · Canada

The Senior Statistical Programmer is responsible for leading programming efforts, including the creation and validation of derived datasets, tables, figures, and listings for clinical trials. They will also oversee deliverables from CROs and contribute to the design and implementation of key statistical documentation and electronic submissions.

Junior Statistical Programmer Analyst _Permanent Role_(CANADA)

Remote · Mississauga, Ontario, Canada

The Junior Statistical Programmer will support the development and validation of clinical trial datasets, tables, figures, and listings. They will collaborate with cross-functional teams to ensure programming outputs meet regulatory standards and project timelines.

Senior Scientist, Risk Management & Safety Surveillance

On-site

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a Senior Scientist, Risk Management & Safety Surveillance on a permanent basis. Responsibilities Position Summary The scientist will be responsible for core safety deliverables including scheduled and ad hoc aggregate reports and will serve as report owner for assigned reports (medium to large volume, standard complexity). He/She will have in-…