Bio-Statistician I

0-2 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: Bio-Statistician I

Experience Required: 0 – 2 Years

Location: [Specify Location]

Job Description:

We are looking for a motivated and detail-oriented Bio-Statistician I to join our team. This is an entry-level position suitable for individuals with 0 to 2 years of experience in statistical analysis, particularly within the clinical research or pharmaceutical industry. As a Bio-Statistician I, you will be responsible for applying statistical methods to support clinical trial data analysis, ensuring that results are accurate, reliable, and comply with regulatory standards.

Key Responsibilities:

Assist in the design and implementation of statistical analysis plans for clinical trials.
Perform statistical analysis of clinical trial data, ensuring that analyses are appropriate and aligned with study objectives.
Generate tables, listings, and figures (TLFs) for clinical trial reports and regulatory submissions.
Collaborate with cross-functional teams, including clinical operations, data management, and programming, to ensure that data analysis needs are met.
Ensure statistical analysis is conducted in compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements.
Provide statistical support for ongoing clinical trials, including monitoring data quality and identifying potential issues.
Assist in the preparation of statistical reports and documentation to support clinical trial findings.
Participate in the review and interpretation of statistical results, helping to provide insights and recommendations.
Stay up to date with new statistical methodologies and software tools to enhance efficiency and improve analysis quality.

Qualifications:

Bachelor’s or Master’s degree in Statistics, Mathematics, Biostatistics, Life Sciences, or a related field.
0-2 years of experience in biostatistics, clinical research, or a related field (internships or academic projects related to clinical trials are a plus).
Strong knowledge of statistical methodologies and concepts commonly applied in clinical trials.
Proficiency in statistical software such as SAS, R, or other relevant tools.
Basic understanding of clinical trial design, data management, and regulatory requirements (e.g., ICH-GCP).
Strong analytical, problem-solving, and data interpretation skills.
Excellent attention to detail and accuracy.
Ability to work effectively in a team environment and communicate findings clearly.
Strong organizational skills and the ability to manage multiple priorities.

This is an excellent opportunity for a new graduate or early-career professional to gain valuable experience in biostatistics and contribute to clinical research efforts. If you are passionate about statistics and want to make an impact in the field of clinical trials, we encourage you to apply.

Rush your CVs to : careers@clinztech.com

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