Senior Regulatory Affairs Manager

Veristat; Northern (KY); Hybrid; USD 125,000 - 160,000; Full time

Benefits offered by this job

Remote work

Flexible time off

Medical insurance

Tuition reimbursement

Retirement plans

Job summary

Veristat is seeking a Senior Regulatory Affairs Manager to guide global regulatory strategy and submissions for healthcare products. You will lead cross-functional teams, advise on agency interactions, and coordinate proactive regulatory planning to expedite clinical trials and marketing approvals.

The ideal candidate has 6–8 years in regulatory affairs within CRO/pharma, with strong knowledge of ICH guidelines, CMC, and excellent communication.

Qualifications

• 6–8 years of regulatory affairs experience in a CRO/pharma setting
• Thorough knowledge of ICH guidelines and regulatory guidelines in relevant territories
• Experience with global regulatory submissions and agency interactions
• Excellent written and oral communication skills and ability to translate regulatory requirements into actionable plans
• Demonstrated ability to lead by example and foster client relationships

Responsibilities

• Lead and manage regulatory submissions and filings for healthcare products
• Provide regulatory strategy guidance and consultation to Veristat clients
• Coordinate cross-functional teams and project timelines
• Communicate with regulatory agencies and manage agency communications

Skills

Regulatory affairs

Client relationships

Regulatory strategy

Cross-functional leadership

Written communication

Education

Bachelor's degree

Advanced scientific degree (PhD or Master)

Tools

Microsoft Word

Microsoft Excel

Job description

## Senior Regulatory Affairs ManagerApply: California: Full time: Posted Today: R-202610899**Job Description:**The Senior Regulatory Affairs Manager manages assigned regulatory and cross-functional projects; provides strategic and operational support to Veristat clients in regulatory decision making processes, filings and maintenance of healthcare products and plays a key role in providing consultation to Veristat’s clients, in translating regulatory requirements into practical application to ensure the success of clinical trials and regulatory submissions. S/he will work with project teams, provide advice on regulatory agency interactions, manage agency communications, support the preparation of submissions, and create strong rapport with clients. **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 teamsLearn more about our core values here!**What we offer*** The estimated hiring range for this role is $125K-160K 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:o Remote workingo Flexible time offo Paid holidayso Medical insuranceo Tuition reimbursemento Retirement plans **What we look for*** Bachelor’s degree in a related field required. Advanced scientific degree (i.e. PhD or Master’s degree) preferred.* 6 - 8 years of regulatory affairs experience in a clinical research organization and/or pharmaceutical setting (or demonstrated ability to function at this level), with a proven track record of global regulatory submissions* As Senior Manager Regulatory Affairs CMC: familiar with manufacturing, specifications, analytical testing and overall regulatory CMC requirements* Thorough knowledge of International Conference on Harmonisation (ICH) guidelines and regulatory guidelines in the relevant territories as well as drug development, clinical trials, and clinical research* Excellent written and oral communication skills including grammatical/technical writing skills, and familiarity with drug development, agency interactions, study designs and regulatory requirements that apply to clinical trials are required* Demonstrated ability to develop and foster positive client relationships.* Demonstrated ability to lead by example and demonstrated skill for technical 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.