Clinical Statistician @ Millicon Consultant

Job Description

locations India - Chennai time type Full time posted on Posted 22 Days Ago job requisition id hidden_mobile

Role Summary:

• Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, standards and best practices.
• Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff.
• Provide statistical expertise on regulatory submissions and ensure quality and appropriateness of submission deliverables under the supervision of senior statistical staff.
• Provide statistical expertise in maximizing the value of aggregate clinical data in support of scientific and drug development strategies under the supervision of senior statistical staff.
• Provide study level statistical expertise and communicate resource needs to management and other line functions for the execution of statistical tasks.

Basic Qualifications:

• Advanced degree (Masters, PhD) in Statistics, Biostatistics, or related field.
• 3-5 yrs. of relevant experience in clinical trials is desirable but not necessary.
• Strong statistical skills with application to clinical trials.
• Effective verbal and written English communication skills in relating to colleagues and associates both inside and outside the organization.
• Working knowledge of SAS, R

Location: Chennai

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical #LI-PFE

Employement Category:

Employement Type: Full time
Industry: Pharma / Biotech
Role Category: General / Other Software
Functional Area: Not Applicable
Role/Responsibilies: Clinical Statistician

Contact Details:

Company: Pfizer
Location(s): Chennai

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Keyskills:   equal employment opportunity clinical data clinical trials drug development communication skills clinical development legislative relations observational studies regulatory submissions regulatory requirements it sas trials english clinical protocols interpret management statements of work sow medical