Strategic Consultant, Biostatistics

Veristat

52d•$200 - $250•Remote

About The Position

Strategic Consultant, Biostatistics This VP level Strategic Consultant drives internal and external consulting efforts, fosters client relationships, and ensures effective service solutions. They contribute to company growth by driving new and expanded business with clients and providing high-quality customer service. They collaborate with clients and business partners to offer expert consultation on clinical trial design, analysis, interpretation, clinical impact, and/or regulatory implications while staying abreast of industry advancements. The Strategic Consultant participates in regulatory meetings as appropriate, business development activities, and mentors cross-disciplinary teams, while exemplifying core values and fostering a positive team environment. Make an Impact at Veristat! Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide. 105+ approved therapies for marketing applications prepared by Veristat 480+ oncology projects in the past 5 years 350+ rare disease projects delivered in the past 5 years Flexible, inclusive culture — 70% remote workforce, 66% women-led teams Learn more about our core values here!

Requirements

PhD or Masters in Statistics, Biostatistics, math-related discipline, or related field, with applied statistics training relevant to clinical trials or health research with expertise in one or more of the following areas: Statistics or Data analytics, Experimental Design and Regulatory Strategy.
12+ years of relevant work experience, preferably with experience in a CRO environment
Thorough knowledge of International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, clinical trials, and clinical research
Demonstrated ability to thoughtfully solve problems, exercise sound judgment, lead by example, and influence without authority
Demonstrated ability to think “big picture” and strategically leverage expertise, to serve as a consultant and business partner with internal and external customers
Excellent written and oral communication skills including grammatical/technical writing skills, and familiarity with moderately complex concepts that apply to Phase I-IV clinical trials and/or regulatory strategy are required
Working knowledge of the relationship and regulatory obligation of the contract research organization (CRO) industry with pharmaceutical / biotech companies
Skilled in use of computer technology and ability to learn new applications
Excellent interpersonal, communication, and organizational skills with the ability to work independently and in a fast paced, team environment

Responsibilities

Drives internal and external consulting efforts
Fosters client relationships
Ensures effective service solutions
Contributes to company growth by driving new and expanded business with clients and providing high-quality customer service
Collaborates with clients and business partners to offer expert consultation on clinical trial design, analysis, interpretation, clinical impact, and/or regulatory implications while staying abreast of industry advancements
Participates in regulatory meetings as appropriate
Participates in business development activities
Mentors cross-disciplinary teams
Exemplifies core values and fostering a positive team environment