Clinical Project Statistician (Pharma / Biostatistics) #ESF4867

ExpertHiring•Indianapolis, IN

60d

About The Position

Global healthcare leader uniting caring with discovery to make life better for people worldwide. Strong focus on innovation, integrity, and inclusion, fostering a people-first culture. Opportunity to impact millions of lives through breakthrough medicines and research. Commitment to employee growth and development with continuous learning and career advancement. If that's you, let's talk! Job Type : Full Time Location : Indianapolis, Indiana Pay : Great Pay! Job Description What you will be doing:

Requirements

Ph.D. in Statistics or Biostatistics with at least 3 years of experience in Clinical Research and Development.
Proficient in statistical programming languages/software such as SAS, R, Spotfire, WinBUGs, etc.
Interpersonal communication skills for effective customer consultation.
Teamwork and leadership skills.
Technical expertise and application with working knowledge of experimental design and statistical analysis.
Self-management skills with a focus on results for timely and accurate completion of competing deliverables.
Resource management skills.
Creativity and innovation.
Demonstrated problem-solving ability and critical thinking.

Responsibilities

Develop or assist in the development of protocol designs, clinical plans, and data analysis plans in collaboration with physicians and clinical research scientists.
Provide input on study protocol, design studies, and write protocols for the conduct of each study.
Select statistical methods for data analysis and author the corresponding sections of the protocol and statistical analysis plan.
Conduct data analysis once a reporting database is created.
Collaborate with data sciences in the planning and implementation of data quality assurance plans.
Maintain proficiency in applying new and varied statistical methodologies.
Perform peer review of work products from other statistical colleagues.
Collaborate with team members to write reports and communicate study results.
Assist or be responsible for communicating study results via regulatory submissions, manuscripts, or oral presentations.
Understand disease states, competitive landscapes, and the regulatory environment to enhance customer focus and collaboration.
Perform work in full compliance with assigned curriculum and follow applicable corporate, medical, local, and departmental policies.
Introduce and apply innovative methodology and tools to solve critical problems.
Lead projects independently and apply technical expertise to influence business decisions.