Catalyst Clinical Services is a leading clinical research organization dedicated to delivering high-quality clinical trial monitoring and management services. With a strong commitment to innovation and patient safety, we specialize in oncology, diabetes, and medical device clinical trials. Our team of experts ensures compliance with regulatory standards and drives successful clinical outcomes.
Job Title: Clinical Research Associate (CRA)
Experience Required: Minimum 2 years in clinical trial monitoring (on-site)
Educational Qualification:
- M.Pharm or Ph.D. in relevant fields
Therapeutic Area Expertise:
- Oncology
- Diabetes
- Medical Devices
Job Description
As a Clinical Research Associate (CRA) at Catalyst Clinical Services, you will play a critical role in the successful execution of clinical trials. Your responsibilities will include:
- Monitoring clinical trial sites to ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
- Conducting on-site visits to assess site performance and data quality.
- Collaborating with investigators, site staff, and internal teams to resolve issues and ensure timely data collection.
- Preparing and maintaining essential documents and reports.
- Ensuring patient safety and data integrity throughout the clinical trial process.
- Supporting the clinical trial team in achieving project milestones and deliverables.
Why Join Catalyst Clinical Services?
- Work with a passionate and experienced team in a dynamic clinical research environment.
- Gain exposure to cutting-edge clinical trials in oncology, diabetes, and medical devices.
- Opportunities for professional growth and development.
- Competitive salary and benefits package.
How to Apply
Interested and eligible candidates are invited to send their updated CV to info@catalystclinicalservices.com. Please mention “Clinical Research Associate Application” in the subject line.
For more information about Catalyst Clinical Services, visit our website: www.catalystclinicalservices.com
