Strategic Consultant

Job Description:

 Strategic Consultant

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 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.

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 $198,000 - $250,000 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 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

Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.

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