Director Regulatory Affairs, responsible for strategic and operational regulatory consulting for client companies. The Director RA will be client facing and will be responsible amongst others for:
Strategic Advice to clients, with focus on early development through to NDA/ BLA
Independent preparation of regulatory documentation such as US IND, NDA/BLA modules, ODD, Fast track / other designations, FDA advice requests.
Scientific Interaction with internal cross functional teams
Client facing & Agency point of contact: Interaction with clients and FDA, lead interactions with Health Authorities
Internal BD & marketing facing role
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
- The estimated hiring range for this role is $195K-223K 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
Bachelor’s degree in science, toxicology, pharmacology, engineering or related field; Advanced Scientific degree such as Master’s degree, Ph.D. or Pharm.D. preferred, with applied training relevant to clinical trials.
10 years of relevant experience working directly for a CRO/ Pharmaceutical Company, with a minimum 5 years of experience leading regulatory development projects.
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.
Excellent written and oral communication skills including grammatical and technical writing skills, and familiarity with moderately complex study designs and regulatory requirements that apply to Phase I-IV clinical trials are required.
In-depth knowledge of the relationship and regulatory obligation of the contract research organization (CRO) industry with pharmaceutical / biotech companies.
Demonstrated ability to lead by example with demonstrated skill for technical and supervisory leadership of staff.
Skilled in use of computer software, including Microsoft Word and Microsoft Excel, and ability to learn new applications.
Excellent interpersonal, communication, and organizational skills with the ability to work independently and in a team environment.
Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Numbers & Facts
Location
Michigan
Website
veristat.com/veristat-culture-our-core-values
Skills
Biotech and Pharmaceuticalunmatched
Clinical Researchunmatched
Clinical Trainingunmatched
Clinical Trialunmatched
Communication Skillsunmatched
Computer Softwareunmatched
Consultingunmatched
Contract Requirementsunmatched
Contract Research Organization (CRO)unmatched
Cross-Functionalunmatched
Customer Relationsunmatched
Diseaseunmatched
Diversityunmatched
Documentationunmatched
FDA (Food and Drug Administration)unmatched
GCP (Good Clinical Practices)unmatched
Health Insuranceunmatched
ICH Regulationsunmatched
Interpersonal Skillsunmatched
Leadershipunmatched
Marketingunmatched
Marketing Softwareunmatched
Medical Terminologyunmatched
Microsoft Excelunmatched
Microsoft Wordunmatched
Oncologyunmatched
Operational Strategyunmatched
Organizational Skillsunmatched
Pharmacologyunmatched
Phase I Clinical Trialsunmatched
Phase IV Clinical Trialsunmatched
Presentation/Verbal Skillsunmatched
Regulationsunmatched
Regulatory Requirementsunmatched
Retirement Planunmatched
Team Playerunmatched
Technical Writingunmatched
Toxicologyunmatched
Writing Skillsunmatched
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