Clinical Data Analyst Iii

4-6 years

Not Disclosed

Hyderabad

10 Jan. 23, 2025

Job Description

Job Type: Full Time Education: B.Sc, M.Sc, B.Pharm, M.Pharm, LifeScience Graduates 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 Analyst III

Experience Required: 4 – 6 Years

Location: [Specify Location]

Job Description:

We are looking for an experienced and skilled Clinical Data Analyst III to join our team. The ideal candidate will have 4 to 6 years of experience in clinical data analysis, with a strong background in managing and interpreting clinical trial data. As a Clinical Data Analyst III, you will play a key role in ensuring the accuracy, integrity, and quality of clinical trial data, supporting decision-making processes and ensuring compliance with regulatory requirements.

Key Responsibilities:

Analyze and interpret clinical trial data to ensure its accuracy, completeness, and consistency.
Review, validate, and clean data from clinical trials to identify and resolve discrepancies, ensuring high-quality data.
Work closely with clinical research teams to provide insights and recommendations based on data analysis to support study objectives.
Develop and implement data management plans, ensuring that data collection, processing, and reporting follow industry standards and regulatory guidelines (e.g., ICH-GCP).
Oversee and mentor junior data analysts, providing guidance and training on best practices in data analysis.
Prepare and deliver reports, presentations, and datasets for internal teams, sponsors, and regulatory bodies.
Ensure compliance with data privacy regulations, industry standards, and sponsor-specific requirements.
Collaborate with cross-functional teams, including clinical operations, biostatistics, and regulatory, to ensure alignment and support of clinical trial goals.
Participate in the development of data analysis strategies, processes, and tools to enhance data management efficiency.
Lead and support the setup, maintenance, and troubleshooting of data management systems and databases.

Qualifications:

Bachelor’s or Master’s degree in Life Sciences, Statistics, Healthcare, or a related field.
4-6 years of experience in clinical data analysis or clinical data management, with a solid understanding of clinical trial processes.
Proficiency in statistical analysis software (e.g., SAS, R) and data management tools (e.g., EDC, CTMS).
Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial data management best practices.
Experience in leading data analysis projects and mentoring junior team members.
Exceptional attention to detail and ability to handle large datasets with accuracy.
Excellent communication and presentation skills, with the ability to effectively communicate complex data findings to cross-functional teams.
Strong problem-solving abilities and ability to resolve data-related issues proactively.
Ability to work effectively in a team-oriented environment and manage multiple priorities.

This is an exciting opportunity for a seasoned Clinical Data Analyst to advance their career and make a significant impact on clinical trial data management. If you have a passion for data integrity and want to contribute to the success of clinical research, we encourage you to apply.

Rush your CVs to : careers@clinztech.com

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Clinical Data Analyst Iii

Job Description

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