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    Clinical Data Coordinator

    Sanofi
    2+ years
    Not Disclosed
    Hyderabad
    10 Oct. 16, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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: Clinical Data Coordinator
    Location: Hyderabad, India
    Grade: L1-1

    About the Job

    At Sanofi, our hubs play a crucial role in driving innovation and enhancing performance across all departments. Join us as a Clinical Data Coordinator within our Clinical Data Management (CDM) Group, where you’ll help transform our business and positively impact millions of lives. Are you ready to get started?

    Major Duties and Responsibilities

    • Ensure data quality through data management activities, including data validation and review, while adhering to study timelines.
    • Monitor the progress of data cleaning activities and generate status reports for the Study Data Manager and study team.
    • Contribute to the writing of study plans, including the Data Management Plan and Centralized Monitoring Plan, in line with timelines defined by the study team.
    • Assist in writing User Acceptance Testing (UAT) Plans and perform testing for databases, listings, patient profiles, and safety notification tools, providing feedback to the programming team and Study Data Manager to collaboratively resolve any issues.
    • Conduct centralized monitoring activities in accordance with the Centralized Monitoring Plan.
    • Maintain clear and consistent communication regarding data management activities at the study level, including risk identification, monitoring, alerts, and escalations.

    About You

    • Experience: Background in clinical data management.
    • Soft Skills: Exceptional attention to detail and accuracy, excellent written and verbal communication skills, and a strong team player who fosters collaboration within CDM and the clinical study team.
    • Technical Skills: Experience with clinical data management and a solid understanding of regulatory guidelines related to data quality and clinical trial conduct. Familiarity with database technologies and the ability to learn new technical skills quickly. Proficient in Microsoft Office Suite (intermediate level).
    • Languages: Good command of English, both spoken and written.
    • Education: Bachelor’s degree or higher, preferably in a life sciences or drug development-related field.

    Why Choose Us?

    • Bring the miracles of science to life alongside a supportive, future-focused team.
    • Discover endless opportunities to grow your talent and advance your career, whether through promotions or lateral moves, at home or internationally.
    • Enjoy a well-crafted rewards package that recognizes your contributions and amplifies your impact.
    • Take care of yourself and your family with a wide range of health and wellbeing benefits, including high-quality healthcare, wellness programs, and at least 14 weeks of gender-neutral parental leave.

    Pursue Progress, Discover Extraordinary

    At Sanofi, progress doesn’t happen without people—individuals from diverse backgrounds, in various roles and locations, united by a desire to create miracles. Join us in chasing change, embracing new ideas, and exploring the opportunities we have to offer.

    We are committed to providing equal opportunities to all, regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

    Watch our One Day at Sanofi video and learn about our Diversity, Equity, and Inclusion initiatives at sanofi.com.

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