1

Live In Fda Scientist Jobs in Boston, MA (NOW HIRING)

Director Regulatory Affairs

Boston, MA · On-site

$163K - $215K/yr

This role owns regulatory direction toward registration, serving as the key voice in FDA interactions and driving INDs, lifecycle strategy, and global submissions. With real autonomy and visibility ...

Regulatory Manager

Gloucester, MA

$120K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Strong expertise in FDA regulations, food labeling, ingredient compliance, and regulatory claims ... Bachelor's degree in Food Science, Microbiology, Public Policy, Legal Studies, or a related ...

Knowledge & Innovation Lawyer - Life Science

Boston, MA · On-site

$85K - $111K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Monitor and proactively alert the Practice of important legal, regulatory and market developments relevant to the Life Sciences practice, including developments in FDA regulation, biologics, clinical ...

Technical Writer

Cambridge, MA · On-site

  • Medical

  • Life

... preferred Knowledgeable in FDA regulations Experienced in Microsoft office applications ... IT Life Sciences Allied Healthcare CRO Certified MBE | GSA - Schedule 66 I GSA - Schedule 621I ...

Senior Director, Regulatory Affairs

Waltham, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

By combining scientific innovation with a collaborative, purpose-driven culture, we strive to ... Deep expertise in FDA regulations and guidance (21 CFR, ICH guidelines), with strong working ...

Senior Director, Regulatory Affairs

Waltham, MA · On-site

$259K - $317K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

By combining scientific innovation with a collaborative, purpose-driven culture, we strive to ... Deep expertise in FDA regulations and guidance (21 CFR, ICH guidelines), with strong working ...

Senior Director, Regulatory Affairs

Waltham, MA · On-site

$259K - $317K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

By combining scientific innovation with a collaborative, purpose-driven culture, we strive to ... Deep expertise in FDA regulations and guidance (21 CFR, ICH guidelines), with strong working ...

Senior Director, Regulatory Affairs

Waltham, MA · On-site

$259K - $317K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

By combining scientific innovation with a collaborative, purpose-driven culture, we strive to ... Deep expertise in FDA regulations and guidance (21 CFR, ICH guidelines), with strong working ...

next page

Showing results 1-20

Live In Fda Scientist information

What is a live in FDA scientist?

A Live In FDA Scientist typically refers to a regulatory scientist who works for the U.S. Food and Drug Administration (FDA) and may be involved in on-site or continuous monitoring of studies, often in clinical or laboratory settings. Their role includes evaluating scientific data, ensuring compliance with federal regulations, and overseeing the safety and efficacy of products such as drugs, biologics, or medical devices. Live-in positions might be required for research facilities needing 24/7 oversight, although such roles are rare and specialized. These scientists play a crucial role in public health by supporting the FDA’s mission to protect consumers.

What are some unique challenges faced by a live in FDA scientist, and how can they be managed?

A Live-In FDA Scientist often works in environments such as research facilities or clinical trial sites where on-site presence is essential. This setup can present challenges like maintaining work-life balance, adapting to extended hours, and managing confidentiality due to the sensitive nature of ongoing research. Successful candidates typically develop strong time management skills, set clear personal boundaries, and foster open communication with team members to ensure both professional responsibilities and personal well-being are balanced. Collaboration with multidisciplinary teams is frequent, and adaptability is key to thriving in this dynamic role.

What are the key skills and qualifications needed to thrive as a live in FDA scientist, and why are they important?

To thrive as an FDA Scientist, you need a strong background in life sciences or chemistry, typically with an advanced degree (MS or PhD) and experience in research or regulatory affairs. Familiarity with laboratory instrumentation, data analysis software, and FDA regulatory systems is essential, and certifications like RAC (Regulatory Affairs Certification) can be advantageous. Attention to detail, critical thinking, and excellent communication skills help you interpret data accurately and collaborate effectively with multidisciplinary teams. These skills ensure scientific integrity, regulatory compliance, and the advancement of public health through safe and effective products.

What is the difference between Live In Fda Scientist vs Fda Reviewer?

AspectLive In Fda ScientistFda Reviewer
Required credentialsBachelor's or Master's in Life Sciences, relevant experienceSimilar credentials, often with advanced degrees
Work environmentOn-site, often in government or research facilitiesOffice-based, reviewing submissions at FDA headquarters or regional offices
Employer and industry usageFederal government, regulatory scienceFederal government, regulatory review
Common search intentJob duties, qualifications, work conditionsComparison of roles, responsibilities, career path

The Live In Fda Scientist and Fda Reviewer roles both require scientific expertise and federal employment credentials. While the Live In Fda Scientist often involves conducting research and scientific analysis on-site, the Fda Reviewer primarily focuses on evaluating regulatory submissions and documentation. Both roles are integral to FDA operations, but they differ in daily tasks and work environment, with the scientist more research-oriented and the reviewer more review-focused.

How much do live in FDA scientists make?

Live-in FDA scientists typically earn a salary comparable to federal scientific positions, which can range from approximately $70,000 to over $130,000 annually depending on experience, education, and location. They often receive benefits such as health insurance and retirement plans, and may work in regulated environments requiring specialized certifications.

What are the most commonly searched types of Fda Scientist jobs in Boston, MA?

The most popular types of Fda Scientist jobs in Boston, MA are:

Regulatory Requirements System Integrity Solutions Director- Life Science

RSM Global

Boston, MA • On-site

$163K - $215K/yr

Full-time

Re-posted 18 days ago


Job description

We are the leading provider of professional services to the middle market globally, our purpose is to instill confidence in a world of change, empowering our clients and people to realize their full potential. Our exceptional people are the key to our unrivaled, culture and talent experience and our ability to be compelling to our clients. You'll find an environment that inspires and empowers you to thrive both personally and professionally. There's no one like you and that's why there's nowhere like RSM.
RSMs Business Application Risk Solutions practice specializes in managing governance, risk, security, data, and compliance across the full lifecycle of core business applications-from implementation through steady-state operations. We help organizations de-risk transformations through independent verification and validations (IV&Vs), or through regulatory requirements system integrity solutions including FDA/GxP/CSA validation and system integration readiness, program risk management, and rigorous data quality validation and analytics. We design and manage integrated and scalable compliant application security solutions. We unlock the power of business applications, enabling automation to manage operational and regulatory compliance risk, or implementing intelligent controls, compliance analytics, and business application GRC solutions.
The Regulatory Requirements System Integrity Solutions Director will be responsible for serving as a strategic advisor helping clients navigate risk and regulatory requirement needs during a business application (SAP, Oracle, NetSuite, Dynamics) implementation in the life-science industry. You would be overseeing a team of solution delivery technical experts of governance, risk, application security, data, controls, with regulatory requirement knowledge, including FDA validation.
Responsibilities:
  • Lead a cross-functional team of subject-matter experts spanning: Governance & compliance, Risk management, Application security, Data governance, IT controls FDA validation & assurance
  • Develop broad service offerings for clients including performing validation strategy assessments focusing on risk, cost, visibility and effectiveness, developing validation strategy master plans, validation SOPs, implementing enabling technology and executing validation testing
  • Ensure application design decisions (configuration, integrations, data model, workflows) incorporate necessary regulatory requirements, compliance, traceability, and control requirements.
  • Review and approve solution designs to ensure alignment with GxP boundaries, regulated vs. non-regulated process flows, and required IT controls.
  • Establish and manage program-wide governance frameworks that ensure integrity, traceability, and compliance throughout the full implementation lifecycle.
  • Drive resolution of regulatory and compliance issues, serving as the escalation point for solution design, validation, or control gaps.
  • Ensure quality of all client deliverables created by the technical SMEs, including risk logs, assessment reports, mitigation plans, design documentation, and testing packages.
  • Direct the creation of governance models, risk and control matrices, access control strategies, and data integrity safeguards across ERP platforms.
  • Lead, mentor, and grow a multidisciplinary team of solution engineers, validation SMEs, GRC specialists, security architects, and data governance professionals.
  • Build and mature internal methodologies, accelerators, templates, and best practices to enhance delivery consistency and efficiency.
  • Drive capability development in FDA validation, ERP controls, and regulatory requirement frameworks within the broader practice.
  • Identify and drive new business opportunities through demonstrating value.
  • Accountable for engagement contracting, financials, including budgeting, forecasting, and financial reporting, to ensure profitability.
  • Effectively communicate program risk to key stake holders along with mitigating solutions across the enterprise and aid in managing resistance through the ability to communicate value and awareness.
  • Develop an optimized delivery structure that will include determining the mix of resources both on, near and offshore as well as working with the team to integrate automation into delivery. Maintain high quality documentation standards

Position Requirements:
  • Proficient in FDA, GxP, and GMP IT validation, as well as other regulatory standards within the life sciences sector.
  • Demonstrated success in interpreting and applying regulatory requirements-including FDA/GxP validation and system readiness-for deploying business systems like SAP, NetSuite, Oracle, and D365 in the Life Sciences industry.
  • Experienced in leading teams with diverse backgrounds and technical expertise. Adept at recognizing the client's actual needs (beyond their stated requests) and developing compelling business cases for optimal solutions within resource limitations.
  • Strong executive presence and excellent communication skills. Strong organizational change management skills
  • Identify opportunities to automate regulatory and validation workflows, including leveraging GRC tools, automated testing tools, and AI-enabled documentation accelerators.
  • Introduce innovative approaches to lifecycle validation, system integrity, and compliance management, especially within modern cloud ERP landscapes.
  • Continuously improve processes around requirements tracking, risk identification, and system assurance.
  • Accountable, self-starter, with the ability to quickly resolve issues and move forward
  • Background in IT auditing would be preferred, but not required.
  • Travel could be up to 25%, based on client needs

Minimum Qualifications:
  • FDA validation readiness experience
  • Education: Undergraduate degree in any one of these areas: entrepreneurship, business administration, program management, business operations, MIS, Accounting, Auditing or other similar degrees
  • Minimum of 12+ years of experience in highly regulated program risk management over large transformations, strong understanding of the software development life cycle
  • Professional certification required, certification for chief of staff would be nice to have but not required.

Standards of Performance:
  • A self-starter with a process improvement mentality who is hands on, results-oriented, and leads by example
  • A strong entrepreneurial spirit with the highest levels of professional and personal honestly, integrity and ethics
  • Excellent organizational skills and the ability to prioritize multiple tasks, projects and assignments
  • Ability to interact with all levels of client staff, including executives and senior managers
  • Possess strong business ethics and willingness to adhere to stringent professional standards
  • Ability to put forth additional effort to meet deadlines when necessary

At RSM, we offer a competitive benefits and compensation package for all our people. We offer flexibility in your schedule, empowering you to balance life's demands, while also maintaining your ability to serve clients. Learn more about our total rewards at https://rsmus.com/careers/working-at-rsm/benefits.
All applicants will receive consideration for employment as RSM does not tolerate discrimination and/or harassment based on race; color; creed; sincerely held religious beliefs, practices or observances; sex (including pregnancy or disabilities related to nursing); gender; sexual orientation; HIV Status; national origin; ancestry; familial or marital status; age; physical or mental disability; citizenship; political affiliation; medical condition (including family and medical leave); domestic violence victim status; past, current or prospective service in the US uniformed service; US Military/Veteran status; pre-disposing genetic characteristics or any other characteristic protected under applicable federal, state or local law.
Accommodation for applicants with disabilities is available upon request in connection with the recruitment process and/or employment/partnership. RSM is committed to providing equal opportunity and reasonable accommodation for people with disabilities. If you require a reasonable accommodation to complete an application, interview, or otherwise participate in the recruiting process, please call us at 800-274-3978 or send us an email at careers@rsmus.com.
RSM does not intend to hire entry level candidates who will require sponsorship now OR in the future (i.e. F-1 visa holders). If you are a recent U.S. college / university graduate possessing 1-2 years of progressive and relevant work experience in a same or similar role to the one for which you are applying, excluding internships, you may be eligible for hire as an experienced associate.
RSM will consider for employment qualified applicants with arrest or conviction records. For those living in California or applying to a position in California, please click here for additional information.
At RSM, an employee's pay at any point in their career is intended to reflect their experiences, performance, and skills for their current role. The salary range (or starting rate for interns and associates) for this role represents numerous factors considered in the hiring decisions including, but not limited to, education, skills, work experience, certifications, location, etc. As such, pay for the successful candidate(s) could fall anywhere within the stated range.
Compensation Range: $141,900 - $286,000
Individuals selected for this role will be eligible for a discretionary bonus based on firm and individual performance.

RSM International logo

About RSM International

Sourced by ZipRecruiter

RSM International is a leading global network of audit, tax, and consulting firms. Headquartered in Chicago, Illinois, US, the firm focuses on providing an exceptional range of professional services to empower clients to move forward with confidence. RSM International was established in 1964 and has since grown to encompass firms in more than 120 countries. The firm's mission is guided by a deep understanding of what clients need to help drive their businesses forward, combined with the international reach of RSM firms worldwide.

Industry

Business management consulting

Company size

10,000+ Employees

Headquarters location

Chicago, IL, US

Social media