Job Description:
Director, Regulatory Affairs
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
- 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
- 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.
Skills Required
- Bachelor's degree in science, toxicology, pharmacology, engineering, or a related field
- Master's degree, Ph.D., or Pharm.D. with applied training relevant to clinical trials
- 10 years of relevant experience working directly for a CRO or pharmaceutical company
- At least 5 years of experience leading regulatory development projects
- Thorough knowledge of ICH Good Clinical Practice guidelines and applicable regulatory rules and guidelines
- Knowledge of medical terminology, clinical trials, and clinical research
- Excellent written and oral communication, grammatical, and technical writing skills
- Familiarity with moderately complex Phase I-IV study designs and applicable regulatory requirements
- In-depth knowledge of CRO regulatory obligations and relationships with pharmaceutical and biotech companies
- Demonstrated technical and supervisory leadership ability
- Proficiency with Microsoft Word and Microsoft Excel, plus ability to learn new applications
- Excellent interpersonal, communication, and organizational skills; ability to work independently and collaboratively
What We Do
Veristat is the science-first full-service drug and biologic CRO and consultancy that integrates strategic planning, regulatory expertise, and clinical trial execution to rapidly advance the most complex or novel therapies. At Veristat, we collaborate with clients to support the rapid delivery of life-changing therapies, helping them make sound decisions amidst uncertainties. Our scientific experts design and conduct the global activities required for any clinical, regulatory, or commercialization program comprehensively and efficiently. With our focus on novel drug development and nearly 30 years of experience, our versatile approach and bold scientific thinking make the impossible possible. Depend on our game-changing expertise and reliable execution for fast results and positive impact to support your biologics and drugs to treat rare cancers, CNS/Neurological disorders, Endocrine/metabolic disorders, and infectious diseases. We are…Bold. Scientific. Versatile. Veristat. - Veristat has recently been made aware that unknown third parties that have no connection to Veristat are generating fake Veristat job postings, interviews, and even fake employment offers via emails, websites, and various social media platforms, seemingly for the purpose of fraudulently obtaining personal information from legitimate job candidates. All legitimate correspondence from Veristat will originate from our applicant tracking system (Jobvite) or an @veristat.com email address. If you have received outreach from someone claiming to be a member of our team please search our official LinkedIn company page (https://www.linkedin.com/company/veristat-llc), where all members of our authorized recruiting team can be identified, or contact us directly at [email protected]. Be vigilant
