Careers
Join our passionate team and help shape the future of global health through innovative research and an unwavering dedication to excellence.
What Employees Are Saying about CCS Associates
“I’m celebrating 25 years at CCSA! The collaborative spirit here is unmatched. Working across several departments and learning from diverse skill sets, has been a fantastic experience. It feels more like a community, not just a workplace.”
“CCSA allows for flex time, though staff are expected to still deliverable high quality documents and services to the client in the expected time frame.”
“I am surrounded by a passionate, collaborative team that truly believes in our mission to shape the future in a positive way.”
“Working at CCSA, you’re surrounded by intelligent people who are passionate about what they do—a refreshingly exceptional combination.”
“It’s a joy to work for a company that cares about its employees, and a real source of pride to be part of such an excellent team.”
“Working at CCSA has given me the chance to be a part of a diverse group of exceptionally talented colleagues in the pursuit of a noble goal. This is a rarity in today’s world, and I’m grateful for the opportunity.”
Join Our Mission
Unlock Your Potential at CCS Associates
CCSA seeks talented, qualified employees in all of our operations. CCSA offers a full benefits package (medical, dental, vision, long-term health), AD&D, life insurance, and 401k plan. CCSA is an Equal Employment Opportunity Employer. CCSA is a remote-first company with team members across the US and Canada. For consideration, send resume, cover letter, and formal writing sample (where requested) to careers@ccsainc.com.
Open Positions
Clinical Research Associate (US-based, East Coast)
Division: Research & Development
Department: Clinical Monitoring
Job Classification: Contract
Reports to: Project Manager, Research & Development
Summary: Provide clinical trial-related monitoring activities including remote and on-site visits to the US sites participating in investigational studies.
Essential Duties and Responsibilities:
- Provides site monitoring support for sponsored clinical studies.
- Performs on-site and remote initiation, routine, and closeout visits.
- Prepares site visit reports and provides assistance to site staff in resolving deficiencies.
- Educates and trains site and study staff in management of sponsored studies, including regulatory and ICH/GCP compliance.
- Collects and processes regulatory documentation for investigational studies in compliance with required guidelines.
- Develops and demonstrates understanding and application of therapeutic area knowledge to assignments and project-related issues.
- Appropriately resolves issues related to trial monitoring and management with guidance from the Project Manager, Clinical Monitoring.
- Makes independent decisions with some supervision from the Senior Director, Research & Development, or the Project Manager, Research & Development.
- Performs primarily intellectual tasks and exercises discretion and independent judgment.
Qualifications:
- Working knowledge of SOPs along with FDA and ICH/GCP guidelines.
- Good communication, organizational, and writing skills.
- Develops and applies efficient computer tools to carry out job functions.
- Attention to detail; ability to work in a team environment.
- Dependable; assumes responsibility and accepts, supports, and positively facilitates change.
- Ability and availability to communicate with sites in different US time zones.
- Willingness to travel.
- Working knowledge of Microsoft Office suite
- Working knowledge of clinical trials electronic tools (CTMS, eTMF, EDC, IRT).
Education and Experience:
- BS/MS/RN or equivalent in scientific or health care field.
- At least 3 years of pharmaceutical, clinical, or biological research with 2 years of Clinical Research Associate experience in oncology.
Clinical Research Associate (US-based, West Coast)
Division: Research & Development
Department: Clinical Monitoring
Job Classification: Contract
Reports to: Project Manager, Research & Development
Summary: Provide clinical trial-related monitoring activities including remote and on-site visits to the US sites participating in investigational studies.
Essential Duties and Responsibilities:
- Provides site monitoring support for sponsored clinical studies.
- Performs on-site and remote initiation, routine, and closeout visits.
- Prepares site visit reports and provides assistance to site staff in resolving deficiencies.
- Educates and trains site and study staff in management of sponsored studies, including regulatory and ICH/GCP compliance.
- Collects and processes regulatory documentation for investigational studies in compliance with required guidelines.
- Develops and demonstrates understanding and application of therapeutic area knowledge to assignments and project-related issues.
- Appropriately resolves issues related to trial monitoring and management with guidance from the Project Manager, Clinical Monitoring.
- Makes independent decisions with some supervision from the Senior Director, Research & Development, or the Project Manager, Research & Development.
- Performs primarily intellectual tasks and exercises discretion and independent judgment.
Qualifications:
- Working knowledge of SOPs along with FDA and ICH/GCP guidelines.
- Good communication, organizational, and writing skills.
- Develops and applies efficient computer tools to carry out job functions.
- Attention to detail; ability to work in a team environment.
- Dependable; assumes responsibility and accepts, supports, and positively facilitates change.
- Ability and availability to communicate with sites in different US time zones.
- Willingness to travel.
- Working knowledge of Microsoft Office suite
- Working knowledge of clinical trials electronic tools (CTMS, eTMF, EDC, IRT).
Education and Experience:
- BS/MS/RN or equivalent in scientific or health care field.
- At least 3 years of pharmaceutical, clinical, or biological research with 2 years of Clinical Research Associate experience in oncology.