Senior Clinical Data Coordinator (Sr. CDC) Hiring at Catalyst Clinical Research
- Exciting Opportunity: Join Catalyst Clinical Research as a Senior Clinical Data Coordinator (Sr. CDC)
- About Catalyst Clinical Research
- Job Responsibilities
- Data Management & Processing
- Regulatory Compliance & Quality Assurance
- Collaboration & Training
- Required Qualifications & Skills
- Education & Experience
- Technical Skills
- Soft Skills
- How to Apply?
- Job Summary Table
Senior Clinical Data Coordinator (Sr. CDC) Hiring at Catalyst Clinical Research
Exciting Opportunity: Join Catalyst Clinical Research as a Senior Clinical Data Coordinator (Sr. CDC)
Are you an experienced clinical data professional looking to advance your career? Catalyst Clinical Research is hiring a Senior Clinical Data Coordinator (Sr. CDC) in Thiruvananthapuram, India. This role offers an excellent opportunity to work with a global clinical research organization, leveraging your expertise in data management and compliance.
About Catalyst Clinical Research
Catalyst Clinical Research is a global CRO specializing in oncology and multi-therapeutic clinical trials. The company provides flexible, customer-centric services, ensuring efficient trial execution with cutting-edge technology and experienced professionals. Catalyst offers a collaborative work environment that fosters professional growth and innovation in clinical research.
Job Responsibilities
As a Senior Clinical Data Coordinator, you will play a crucial role in managing and processing clinical trial data to ensure accuracy, consistency, and compliance with regulatory requirements. Your key responsibilities include:
Data Management & Processing
- Develop, validate, and maintain clinical trial data within Electronic Data Capture (EDC) systems.
- Conduct User Acceptance Testing (UAT) on eCRF builds and edit specifications.
- Perform manual data listing reviews, generating queries where necessary.
- Manage query resolution to maintain data integrity.
Regulatory Compliance & Quality Assurance
- Ensure compliance with ICH-GCP guidelines and company SOPs.
- Collaborate with the Global Drug Safety team to reconcile Serious Adverse Events (SAE).
- Assist in preparing safety reports and regulatory documentation.
- Support internal and external audits by providing necessary data insights.
Collaboration & Training
- Work closely with clinical research teams, site coordinators, and biostatisticians.
- Assist in eCRF design and review.
- Provide training and mentorship to junior data coordinators.
- Support study report generation for regulatory submissions.
Required Qualifications & Skills
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📱 Get More DetailsTo qualify for this role, you must have:
Education & Experience
- Bachelor’s degree in Life Sciences, Biotechnology, Pharmacy, or a related field.
- Minimum 3+ years of experience in clinical data management.
Technical Skills
- Proficiency in Electronic Data Capture (EDC) systems.
- Strong knowledge of Microsoft Office Suite, SAS, and clinical data software.
- Familiarity with clinical trial regulations (ICH-GCP, FDA, EMA).
Soft Skills
- Strong analytical and problem-solving abilities.
- Excellent communication and collaboration skills.
- Ability to manage multiple projects and meet deadlines.
How to Apply?
If you are passionate about clinical research and data management, apply today! Click the link below to submit your application:
Job Summary Table
| Company Name | Catalyst Clinical Research |
|---|---|
| Current Vacancies | Senior Clinical Data Coordinator (Sr. CDC) |
| Required Education | Bachelor’s degree in Life Sciences, Biotechnology, Pharmacy, or a related field |
| Experience Required | Minimum 3+ years in Clinical Data Management |
| Location | Thiruvananthapuram, India |
To apply for this job please visit ats.rippling.com.