Senior Clinical Data Coordinator

3+ years

Not Disclosed

Hyderabad

10 Dec. 3, 2024

Job Description

Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Senior Clinical Data Coordinator
Location: Hyderabad, India

About the Job:
As a Senior Clinical Data Coordinator (CDC), you will play a pivotal role in ensuring the accuracy, completeness, and consistency of clinical databases during the course of studies, adhering to Good Clinical Practices (GCP) and regulatory guidelines. Working as part of our Clinical Data Management team, you will support the Study Data Manager in meeting study timelines and maintaining data quality. Your contributions will directly impact the success of our studies and the lives of patients worldwide.

Key Responsibilities:

Data Management Activities: Ensure data quality by performing tasks such as data validation, review, and centralized monitoring in alignment with study timelines.
Progress Monitoring: Track data cleaning activities and generate status reports for the Study Data Manager and study team.
Documentation: Contribute to study documentation, including Data Management Plans, Centralized Monitoring Plans, and other study-related documents.
User Acceptance Testing (UAT): Develop UAT plans, test databases, listings, patient profiles, and safety notification tools, and collaborate with programming teams to resolve any issues.
Centralized Monitoring: Conduct monitoring activities as outlined in the Centralized Monitoring Plan and communicate effectively on study-level data management activities, including risk identification and escalation.
Mentorship: Act as a mentor for new Clinical Data Coordinators and identify opportunities for process improvement and increased data quality.
Support Functions: Provide backup support to the Study Data Manager as needed and contribute to new initiatives within data management activities.

About You:

Experience:

Previous experience in Clinical Data Management with a strong understanding of regulatory guidelines related to data quality and clinical trial conduct.

Soft Skills:

Attention to detail and accuracy.
Excellent written and verbal communication skills.
Strong team player with a collaborative mindset.

Technical Skills:

Proficiency in clinical data management systems and tools.
Familiarity with database technologies and the ability to learn new technical skills.
Competence in Microsoft Office Suite (intermediate level).

Education:

Bachelor’s degree or higher, preferably in life sciences or a related field.

Languages:

Proficiency in English, both verbal and written.

Why Join Us?

Be part of a transformative team bringing the miracles of science to life.
Explore endless opportunities for career growth, including promotions, lateral moves, and international assignments.
Enjoy a comprehensive rewards package that recognizes your contributions.
Contribute to the modernization and innovation of Clinical Data Management.

“Sanofi is at the forefront of Clinical Data Management Modernization. Join us to help turn our vision into reality.”

Diversity and Inclusion at Sanofi:
At Sanofi, we are committed to fostering a diverse and inclusive environment. We provide equal opportunities to all individuals, regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Discover more about our Diversity, Equity, and Inclusion initiatives and what it’s like to work at Sanofi at sanofi.com.

Apply Now
Join us in pursuing progress and discovering extraordinary together.

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Senior Clinical Data Coordinator

Job Description

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