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Experienced Biostatistics Consultant - Remote

Posted 12 weeks ago
All others
Full Time
USA

Overview

Join MMS, a data-focused clinical research organization, as an Experienced Biostatistics Consultant. Contribute to innovative projects in a supportive environment while shaping the future of clinical research.

In Short

  • Serve as study statistician for assigned studies.
  • Create randomization and kit schedules independently.
  • Provide input in study design and statistical methodologies.
  • Develop SAPs and iSAPs with no supervision.
  • Review/validate ADaM and SDTM specifications and files.
  • Lead complex projects and manage client meetings.
  • Familiar with industry practices and regulatory guidelines.
  • Support Data Safety Monitoring Boards as unblinded statistician.
  • High proficiency with MS Office applications.
  • Provide statistical expertise as needed.

Requirements

  • Masters in Biostatistics or related field, PhD preferred.
  • Minimum of 7 years’ experience in Biostatistics or similar field.
  • Expert knowledge of scientific principles and concepts.
  • Proficiency with MS Office applications.
  • Hands-on experience with clinical trial and pharmaceutical development preferred.
  • Good communication and problem-solving skills.
  • Familiarity with ISO 9001 and ISO 27001 standards preferred.
  • Familiarity with FDA and GCP requirements.
  • Basic understanding of CROs and drug development process.

Benefits

  • Great Place to Work certified organization.
  • Exceptional culture and employee retention rate.
  • Collaborative and inclusive work environment.
  • Opportunities for career advancement.

MMS

MMS

MMS is an award-winning, data-focused clinical research organization (CRO) that supports the pharmaceutical, biotech, and medical device industries. Recognized as a Great Place to Work certified organization, MMS boasts an exceptional culture and industry-leading employee retention rate. With a global presence across four continents, the company excels in providing scientific solutions to complex trial data and regulatory submission challenges. MMS is committed to fostering a collaborative and inclusive work environment, ensuring that employees can thrive while contributing to the future of clinical research.

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