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VP, Regulatory Affairs, Strategy

Employer
Syner-G BioPharma Group
Location
Working from Home
Start date
Oct 30, 2024
View more categoriesView less categories
Discipline
Marketing, Regulatory, Regulatory Affairs
Required Education
Masters Degree/MBA
Position Type
Full time

Job Details

COMPANY OVERVIEW:

 

Syner-G BioPharma Group and Sequoia Biotech Consulting recently merged in September 2024, uniting two industry leaders to create a new force in life sciences consulting. By combining our expertise in product development, regulatory strategy, quality and compliance and commercial manufacturing, we are positioned to deliver fully integrated solutions across the development continuum.
 
We are helping to enhance human health. This merger strengthens our ability to accelerate groundbreaking therapies and help clients navigate the complex life sciences landscape with greater agility and confidence. Together, we form a leading life sciences consultancy dedicated to empowering organizations to overcome complex challenges and accelerate the speed to market, scale and quality of life-saving innovations. 

We work across a diverse range of clients and projects, supporting many organizations through the most critical phases of the drug discovery, approval, product development, technology transfer and commercial manufacturing process. We also equip our partners with the tools, knowledge and expertise to streamline operations, enhance quality and ensure compliance.

Syner-G BioPharma Group was recently honored with BioSpace's prestigious "Best Places to Work" 2025 award, for the second consecutive year, along with many other award winning programs to make a career here truly life-enhancing. These recognitions are a testament to our commitment to fostering a positive and engaging work environment for our employees, with a particular emphasis on culture, career growth and development opportunities, financial rewards, leadership and innovation.

At Syner-G and Sequoia, we recognize that our team members are our most valuable asset. Join us in shaping the future, where your talents are valued, and your contributions make a meaningful impact.

POSITION OVERVIEW:

The VP, Regulatory Affairs, Strategy is a senior leadership role responsible for guiding clients through complex regulatory processes, particularly in clinical development and application filings. This role oversees the development and execution of regulatory strategies across various modules, ensures compliance with FDA and international guidelines, and drives business growth through client engagement and business development activities. This position will work cross functionally with CMC technical, QA/Compliance and Medical writing teams to enable timely filing and successful development and regulatory approval of life-saving drugs.

 

WORK LOCATION:

This position is eligible for remote work based on company requirements, with no minimum in-office requirement. Domestic and international travel may be required for this position (Up to 20%).

JOB FUNCTIONS:

(This list is not exhaustive and may be supplemented and changed as necessary.)

  • Guide clients on strategic decisions, agency meetings, and regulatory filings, with emphasis on clinical development, BLA preparations, and compliance.
  • Develop, review, and implement regulatory strategies across all modules (clinical, non-clinical, labeling, drug substance, and drug product).
  • Lead business development activities, including client outreach, webinars, marketing materials, and scoping calls, while identifying new opportunities for growth.
  • Oversee regulatory submissions (i.e., INDs, BLA, NDA) and provide Non-Clinical/Clinical leadership, ensuring compliance with FDA and international requirements.
  • Be the Regulatory Lead on behalf of the client for FDA/Health Authority interactions on key topics/issues during the entire lifecycle of drug development (Pre-IND to NDA/BLA approval). 
  • Mentor and lead a team of regulatory professionals, managing staffing, resource allocation, and talent development.
  • Act as a client lead, handling communications, regulatory strategy, and engagement across multiple projects.
  • Collaborate with clients and internal teams to ensure alignment on timelines, strategy, and regulatory communications.
  • Support vertical heads with financial reporting and profitability tracking across client accounts.
  • Actively participate in external professional meetings (e.g. DIA/RAPS) communicating innovative strategies and thought leadership to advance drug development.

 

QUALIFICATIONS AND REQUIREMENTS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the education, experience, skills, knowledge, and abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform essential duties.

Education: 

  • Advanced degree (e.g. Ph.D, or Pharm.D. or MS) in a relevant scientific discipline; Regulatory certification preferred.

 

Technical Experience:

  • Extensive experience (15+ years) in regulatory affairs, including agency interactions and strategic regulatory planning.
  • Experience in leading teams in filing of INDs and NDAs/BLAs all the way to successful approval and launch of commercial products.
  • Expertise across all phases of drug development, including biologics, pharmaceuticals, oncology, orphan drugs, and pediatric studies.
  • In-depth knowledge of FDA regulations, international guidelines, and the ability to advise on fast-track analysis, pediatric studies, and emergency inquiries.
  • Strong project management skills, with a proven ability to lead teams, prioritize multiple projects, and maintain compliance across global submissions.
  • Broad technical knowledge and experience in managing small and large molecules, including innovative regulatory strategies

 

Knowledge, Skills, and Abilities:

  • Proven leadership experience in managing teams, projects, and client relationships within a pharmaceutical or biotech environment.
  • Strong communication skills, with the ability to mentor, educate, and influence a diverse group of stakeholders.
  • Ability to work in a fast-paced, dynamic environment, managing multiple projects and clients while ensuring regulatory compliance and alignment with business goals.
  • Proven leadership and experience in designing the strategy and leading Health Authority interactions to achieve successful outcome.  
  • Business acumen, with a focus on business development, marketing, sales support, and client engagement.
  • Strong leadership and people management skills, fostering collaboration, consensus-building, and team development.

 

 

ESSENTIAL FUNCTIONS: 

Physical Demands:

The physical demands described here are representative of the requirements that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is regularly required to use a computer keyboard and mouse; reach with hands and arms; talk and listen. The employee is frequently required to walk and sit. The employee is occasionally required to stand, stoop, or kneel. Specific vision abilities required by this position include close vision and the ability to adjust focus.

Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job, including moderate noise level, an indoor temperate environment, and light levels that are bright and conducive to minimal eye strain, typical for an office environment.

 

TOTAL REWARDS

We define total rewards as compensation, benefits, remote work/flexibility, development, recognition and our culture with programs that support each of our reward pillars.  This includes a market competitive base salary and annual incentive plan, robust benefit offerings, and ongoing recognition and career development opportunities. Employees also enjoy our generous flexible paid time off program, company paid holidays, flexible working hours, and fully remote work options for most positions and the ability to work “almost anywhere”. However, if a physical work location is more for you, we have office locations in Greater Boston; San Diego, CA; Boulder, CO; and India.


EQUAL EMPLOYMENT OPPORTUNITY EMPLOYER

Syner-G BioPharma Group and Sequoia Biotech Consulting are proud to be an Equal Employment Opportunity and Affirmative Action employers. All employment decisions, including the recruiting, hiring, placement, training availability, promotion, compensation, evaluation, disciplinary actions, and termination of employment (if necessary) are made without regard to the employee’s race, color, creed, religion, sex, pregnancy or childbirth, personal appearance, family responsibilities, sexual orientation or preference, gender identity, political affiliation, source of income, place of residence, national or ethnic origin, ancestry, age, marital status, military veteran status, unfavorable discharge from military service, physical or mental disability, or on any other basis prohibited by applicable law. Syner-G BioPharma is an E-Verify employer.

 

Applicants must have current work authorization when accepting a position at Syner-G. Currently, Syner-G is unable to sponsor or take over sponsorship of an employment Visa at this time.

 



Company

Syner-G Bio Pharma Group is an organization with roots to the Greater Boston area started by industry leaders in 2007 who saw a niche in the pharmaceutical consulting space and leveraged their subject matter expertise and industry knowledge to grow an organization through hard work, trusted relationships, a collaborative approach, and delivering best in class client services, growing the company and geographical footprint across the globe to be an industry leader in integrated biopharma consulting services across the CMC, Regulatory Affairs and Medical Writing verticals supporting small molecule, biologics and medical device development and delivery. Key values of collaboration, a one-team mindset, and benevolence were not only the cornerstone of initial success, but also the culture that has been created since our founding, placing our people at the center of our company.

As an employee, you will experience us leading with our core mission, “To develop and inspire pharmaceutical consulting professionals”. We encourage open, two-way communication throughout the company and provide a supportive and encouraging working environment that allows employees to reach their greatest potential, celebrating those who live our values every day. We realize the vital role a positive work/life balance plays in establishing a rewarding, productive, and long-term career. As a result, a flexible, family-friendly work environment is a key element of our culture and is one of the reasons people want to work (and stay) here!

We offer an outstanding total rewards package, including a competitive base salary and annual incentive plan, robust benefit offerings, and ongoing recognition and career development opportunities. Employees also enjoy our generous unlimited paid time off program, 13 paid holidays, flexible working hours, and fully remote work options for most positions and the ability to work “almost anywhere”. However, if a physical work location is more for you, we have locations in Greater Boston, Raleigh, NC, Boulder, CO, and Chennai, India.

 

CONNECT

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Company info
Website
Phone
508.460.9700
Location
100 Pennsylvania, Ave, Suite 310
Framingham
MA
01701
US

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