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Vice President, Regulatory Affairs

In Navarra United States

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Vice President, Regulatory Affairs   

JOB TITLE:

Vice President, Regulatory Affairs

JOB TYPE:

Full-time

JOB LOCATION:

Raleigh Navarra United States

JOB DESCRIPTION:

Precision for Medicine is not your typical CRO.
At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients.
What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences.

As our organisation continues to grow we are looking for a Vice President, Regulatory Affairs who will provide worldwide, strategic leadership in and comprehensive understanding of the government regulatory requirements for product development utilizing regulatory knowledge and expertise to ensure regulatory compliance.

Essential functions of the job include but are not limited to:

  • Regulatory Oversight / Intelligence
  • Develop and implement strategies for the timely preparation and execution of regulatory documents to regulatory authorities for contracted programs.
  • Provide expert analysis and evaluation of regulatory information.
    Informs the teams (internal and external stakeholders, as needed) of the regulatory status of products / programs and significant regulatory issues.
  • Provides analysis of regulatory guidance documents, regulations or directives that influence Precision's operations and impacted programs.
    Advises other departments as well as external stakeholders regarding their applicability and impact.
  • Develop and maintain current regulatory knowledge and ensure that staff is aware of new and existing relevant procedures.
  • Develop global regulatory strategy(s) for contracted clinical programs to ensure successful initiation, execution and submission for global registration.
  • Lead and/or facilitate team preparation for regulatory agencies/Health Authority meetings.
  • Lead and/or facilitate communications with regulatory agencies.
  • Preparation of briefing and regulatory documents for regulatory agencies, such as Dossiers, NDAs, INDs/BLAs, and Annual reports
  • Provide oversight to study teams regarding regulations/guidelines and company SOPs to ensure successful and high-quality regulatory applications.
  • Lead, oversee and coordinate critical reviews and provide strategic input on regulatory filing documents (e.
    g.
    , eCTD Module 2 summaries, integrated summary documents, statistical analysis plans and clinical study reports)
  • Lead and facilitate development of any USPI/SmPC labeling activities with cross functional teams for planned regulatory submission.
    Department Oversight / Leadership
  • Provide guidance and leadership to the members of the Regulatory Affairs department.
  • Develop, define and lead internal growth and resourcing strategy for Regulatory Affairs within the organization and direct and oversee all regulatory staff.
  • Oversee the development and management of the regulatory infrastructure.
  • Develop and manage a global budget and resourcing supporting Regulatory Affairs department.
  • Hire, mentor, and support the personal and professional development of regulatory staff.
  • Lead Regulatory Affairs business development activities.
  • Contribute to development of regulatory consulting business to support client development and growth, to achieve an initial annual sales target for regulatory-specific work (outside of clinical trial support)

Qualifications:

Minimum Required:

  • Bachelor's degree in life sciences or medicine
  • 15+ years relevant regulatory and/or clinical development pharmaceutical/biotechnology experience Mastery knowledge of all aspects of the drug development process inclusive of regulatory milestones
  • Significant experience in all aspects of meeting with Regulatory/Health Authorities supporting drug development.
  • Ability to apply knowledge of FDA, EMA Global Health Authority requirements and ICH guidelines both strategically and operationally and provide direction to resolve complex regulatory issues.
  • Prior experience in developing successful global development strategies of cutting edge and unique therapies.
  • Expertise in preparing complex regulatory documents including INDs, milestone briefing packages (EOP2, EOP3, pre-NDA/BLA, Scientific Advice), NDAs/BLAs, and other major regulatory submission.
  • Prior experience in business development activities
  • Availability for domestic and international travel including overnight stays.

Preferred:

  • Advanced degree
  • Experience growing and managing a global regulatory function CRO and Pharma experience preferred.
  • Prior work experience in haematology/oncology
  • Ability to understand clinical and pre-clinical study results, to help in its interpretation for global regulatory positions and strategy.
  • Ability to manage multiple and varied tasks in a fast-moving environment, good record-keeping skills.
  • Strong interpersonal and client-facing skills and a proven ability to contribute to a team environment involving balancing the demands stemming from a variety of multifaceted research activities, demanding regulatory requirements, budgetary responsibility, commitment to highest quality and the requirements of business development and pharmaceutical collaborating are necessary.
  • Proven ability to communicate with management, external thought-leaders and operational staff.
  • Ability to guide, train and supervise personnel; oversees the work of direct reports to ensure ontime, on target and within budget results.
  • Flexible attitude with respect to work assignments, and new learning opportunities

At Precision for Medicine, we believe that the era of one-size-fits-all medication is giving way to a next generation of treatments, medicines that will be more effective because they are prescribed according to the unique biology of an individual patient.
Our mission is to help innovative biotech and pharmaceutical companies accelerate the development of these life-changing treatments.
Precision does this by developing assays that utilize biomarkers to help identify the right patient for the right drug.
We handle every aspect of clinical trials from initial strategy and design to selecting sites and executing quality clinical trials.
This is where you come in!

We invite you to learn more about our growing organization serving our clients that are researching ground breaking cancer therapies.
We strive to ensure employees feel appreciated for the contributions they make every single day.
You will provide input and have your ideas valued and nurtured, impacting positive change for the company.

#LI-NC1 #LI-Remote


Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role.
This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs.
The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled.
At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case.
This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

Reasonable estimate of the current range

$102,500$138,700 USD

Any data provided as a part of this application will be stored in accordance with our Privacy Policy.
For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer.
Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
2020 Precision Medicine Group, LLC

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.
com.

Position Details

POSTED:

EMPLOYMENT:

Full-time

SALARY:

138700 per year

SNAPRECRUIT ID:

S-1707361394-1821bad9623a955444b573110762e990

LOCATION:

Navarra United States

CITY:

Raleigh

Job Origin:

jpick2

A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Vice President, Regulatory Affairs    Apply

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Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences.

As our organisation continues to grow we are looking for a Vice President, Regulatory Affairs who will provide worldwide, strategic leadership in and comprehensive understanding of the government regulatory requirements for product development utilizing regulatory knowledge and expertise to ensure regulatory compliance.

Essential functions of the job include but are not limited to:

  • Regulatory Oversight / Intelligence
  • Develop and implement strategies for the timely preparation and execution of regulatory documents to regulatory authorities for contracted programs.
  • Provide expert analysis and evaluation of regulatory information. Informs the teams (internal and external stakeholders, as needed) of the regulatory status of products / programs and significant regulatory issues.
  • Provides analysis of regulatory guidance documents, regulations or directives that influence Precision's operations and impacted programs. Advises other departments as well as external stakeholders regarding their applicability and impact.
  • Develop and maintain current regulatory knowledge and ensure that staff is aware of new and existing relevant procedures.
  • Develop global regulatory strategy(s) for contracted clinical programs to ensure successful initiation, execution and submission for global registration.
  • Lead and/or facilitate team preparation for regulatory agencies/Health Authority meetings.
  • Lead and/or facilitate communications with regulatory agencies.
  • Preparation of briefing and regulatory documents for regulatory agencies, such as Dossiers, NDAs, INDs/BLAs, and Annual reports
  • Provide oversight to study teams regarding regulations/guidelines and company SOPs to ensure successful and high-quality regulatory applications.
  • Lead, oversee and coordinate critical reviews and provide strategic input on regulatory filing documents (e.g., eCTD Module 2 summaries, integrated summary documents, statistical analysis plans and clinical study reports)
  • Lead and facilitate development of any USPI/SmPC labeling activities with cross functional teams for planned regulatory submission. Department Oversight / Leadership
  • Provide guidance and leadership to the members of the Regulatory Affairs department.
  • Develop, define and lead internal growth and resourcing strategy for Regulatory Affairs within the organization and direct and oversee all regulatory staff.
  • Oversee the development and management of the regulatory infrastructure.
  • Develop and manage a global budget and resourcing supporting Regulatory Affairs department.
  • Hire, mentor, and support the personal and professional development of regulatory staff.
  • Lead Regulatory Affairs business development activities.
  • Contribute to development of regulatory consulting business to support client development and growth, to achieve an initial annual sales target for regulatory-specific work (outside of clinical trial support)

Qualifications:

Minimum Required:

  • Bachelor's degree in life sciences or medicine
  • 15+ years relevant regulatory and/or clinical development pharmaceutical/biotechnology experience Mastery knowledge of all aspects of the drug development process inclusive of regulatory milestones
  • Significant experience in all aspects of meeting with Regulatory/Health Authorities supporting drug development.
  • Ability to apply knowledge of FDA, EMA Global Health Authority requirements and ICH guidelines both strategically and operationally and provide direction to resolve complex regulatory issues.
  • Prior experience in developing successful global development strategies of cutting edge and unique therapies.
  • Expertise in preparing complex regulatory documents including INDs, milestone briefing packages (EOP2, EOP3, pre-NDA/BLA, Scientific Advice), NDAs/BLAs, and other major regulatory submission.
  • Prior experience in business development activities
  • Availability for domestic and international travel including overnight stays.

Preferred:

  • Advanced degree
  • Experience growing and managing a global regulatory function CRO and Pharma experience preferred.
  • Prior work experience in haematology/oncology
  • Ability to understand clinical and pre-clinical study results, to help in its interpretation for global regulatory positions and strategy.
  • Ability to manage multiple and varied tasks in a fast-moving environment, good record-keeping skills.
  • Strong interpersonal and client-facing skills and a proven ability to contribute to a team environment involving balancing the demands stemming from a variety of multifaceted research activities, demanding regulatory requirements, budgetary responsibility, commitment to highest quality and the requirements of business development and pharmaceutical collaborating are necessary.
  • Proven ability to communicate with management, external thought-leaders and operational staff.
  • Ability to guide, train and supervise personnel; oversees the work of direct reports to ensure ontime, on target and within budget results.
  • Flexible attitude with respect to work assignments, and new learning opportunities

At Precision for Medicine, we believe that the era of one-size-fits-all medication is giving way to a next generation of treatments, medicines that will be more effective because they are prescribed according to the unique biology of an individual patient. Our mission is to help innovative biotech and pharmaceutical companies accelerate the development of these life-changing treatments. Precision does this by developing assays that utilize biomarkers to help identify the right patient for the right drug. We handle every aspect of clinical trials from initial strategy and design to selecting sites and executing quality clinical trials. This is where you come in!

We invite you to learn more about our growing organization serving our clients that are researching ground breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company.

#LI-NC1 #LI-Remote


Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

Reasonable estimate of the current range

$102,500$138,700 USD

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. 2020 Precision Medicine Group, LLC

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.


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