The 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 highquality 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 crossdisciplinary teams while exemplifying core values and fostering a positive team environment.
What We Do
For more than 30 years Veristat has built a reputation as global experts in clinical development.
760 Rare Disease Clinical Trials supported
160 Marketing Applications supported
In 2022 we supported 8 marketing application that received regulatory approval
Learn more about our core values here!
What We Offer
The estimated hiring range for this role is $198000 $250000 plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors including but not limited to: skills and experience licensure and certifications education specific location and dynamic market data.
Benefits vary by location and may include:
Remote working
Flexible time off
Paid holidays
Medical insurance
Tuition reimbursement
Retirement plans
What We Look For
PhD or Masters in related discipline with applied training and experience relevant to clinical trials or health research with expertise in one or more of the following areas: Medicine Statistics or Data analytics Pharmacology Regulatory Strategy
10 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 IIV 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
Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decisionmaking process.
Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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