At a Glance
- Tasks: Lead high-quality projects in regulatory affairs and collaborate with diverse teams.
- Company: Join Veristat, a global leader in accelerating life-changing therapies.
- Benefits: Enjoy remote work, flexible time off, and tuition reimbursement.
- Other info: Inclusive culture with 70% remote workforce and strong career growth opportunities.
- Why this job: Make a real impact on patient therapies while growing your career.
- Qualifications: Bachelor’s degree and 6-8 years of regulatory experience required.
The predicted salary is between 128000 - 144000 $ per year.
Senior Project Manager, Regulatory Affairs provides management and leadership to plan, prepare, and execute high quality projects. S/he interfaces with internal departments and company leadership, and externally with sponsors and vendors. The Senior Project Manager, Regulatory Affairs will integrate consulting activities and assignments across all areas of consulting conducted (CMC, quality, regulatory, clinical and business) in coordination with other teams.
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
What We Offer
The estimated hiring range for this role is $128 – 144K plus applicable bonus. This hiring range is specific to the USA 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 life/health sciences or related discipline, or equivalent required.
- 6 to 8 years of relevant Regulatory experience in a Clinical Research Organization/Pharmaceutical Company, with a minimum of 3 years of Project Management or functional team lead experience required.
- Excellent written and oral communication and interpersonal skills, as well as strong planning and organizational ability are required.
- Good working knowledge of drug development process and regulatory requirements, including familiarity with International Conference on Harmonisation (ICH) guidelines and other applicable regulatory rules and guidelines.
- Proficiency in English (written and verbal).
- Action-oriented and resilient in a fast-paced environment and will have the ability to build effective project teams, motivate others, delegate, and make and implement decisions.
- Ability to build and maintain trust and confidence and communicate effectively with client, external vendors, and internal team members.
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.
Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Senior Project Manager, Regulatory Affairs in Québec employer: Veristat
Veristat is an exceptional employer that fosters a collaborative and inclusive work environment, allowing employees to thrive in their roles while making a significant impact in the regulatory affairs landscape. With a focus on professional growth and development, team members benefit from flexible working arrangements and the opportunity to engage with diverse client projects, all while contributing to meaningful advancements in healthcare. Located in a global setting, Veristat offers a unique chance to work alongside industry leaders and shape the future of regulatory strategy.
