Search jobs > Boston, MA > Director writing

Associate Director, Clinical Regulatory Writing (Hybrid)

myGwork
Boston, MA, United States
$157.6K-$236.4K a year
Full-time

This inclusive employer is a member of myGwork the largest global platform for the LGBTQ+ business community.

Job Description

At Vertex, our Clinical Regulatory Medical Writers are strategic scientific partners in the drug development process, collaborating with cross-functional teams to bring new, life-changing products to patients.

The Associate Director, Clinical Regulatory Medical Writing manages the overall operations of a team or major project and implements this through effective leadership.

This role provides guidance and leadership for document development for regulatory filings and coordinates the clinical sections of more complex regulatory submissions, including organization, content, and resource requirements.

This role applies advanced technical expertise and develops solutions to complex problems, fosters interdisciplinary understanding, and integrates Medical Writing Science department activities with those of other departments.

Key Duties and Responsibilities :

  • Independently authors routine and complex clinical and regulatory documents
  • Provides strategic input into program-level plans
  • Deep insight into how different functions contribute to the successes of the team
  • Aligns, coordinates, and builds consistent information and messages across clinical program(s)
  • Provides leadership related to the activities of Medical Writing Science and manages a team
  • Participates in developing and implementing goals and initiatives for Medical Writing Science
  • Facilitates implementation of new technologies and initiatives related to the preparation of clinical documents
  • Proactively anticipates risks, solves complex problems, and seeks out and implements process improvements

Knowledge and Skills :

  • Demonstrated aptitude for planning, managing, and optimizing department resources (e.g., staff, technology) to maximize and streamline the advancement of company goals and objectives
  • Record of leadership, independence, and ability to solve non-routine, complex problems involving a broad range of issues
  • Proven track record of anticipating potential problems and preparing contingency plans as needed
  • Understanding of scientific disciplines beyond own specialty area
  • Experience managing direct reports and guiding staff development
  • Experience with marketing authorization application regulatory submissions

Education and Experience :

  • Ph.D. in a relevant field
  • Typically requires 8 years of work experience and 2 years of supervisory / management experience, or the equivalent combination of education and experience

Pay Range 157,600.00 - 236,400.00 USD annually

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting.

This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements.

Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.

From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

LI-AR1

LI-Hybrid

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law.

Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and / or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at [email protected].

19 days ago
Related jobs
Promoted
Boston Medical Center
Boston, Massachusetts

The VIAP Associate Clinical Director, will work collaboratively with the VP of Hospital Mission and the VIAP Clinical Director and has the primary responsibility of supporting all aspects of program administration and operation, including financial and grants management, strategic planning, personne...

Promoted
Lantheus
Bedford, Massachusetts

The Medical Director Clinical Research will report to the Senior Medical Director, Clinical Research and be responsible for the design and interpretation of Lantheus clinical studies, including protocol development and oversight. Contribute to authoring and lead design/reviews of key product and stu...

Promoted
Alnylam Pharmaceuticals
Cambridge, Massachusetts

Associate Director, Clinical Trial Oversight will provide strong leadership and clinical operations experience to support Alnylam's oversight of CRO monitoring effectiveness. The Associate Director, Clinical Trial Oversight will manage Clinical Trial Oversight Leads (CTOLs) and direct the work of FS...

Promoted
Cornerstone Search Group
Boston, Massachusetts
Remote

Strong ability to partner with other functions, including preclinical, early-stage clinical development, clinical operations, regulatory, and external collaborators. Senior Director, Late-stage Clinical Development | MD Leadership | Successful Commercial Hematology/Oncology Biotech | Great Culture |...

Promoted
Biotech
Boston, Massachusetts

We are seeking a strategic and experienced Associate Director/Director of Clinical Operations to lead our clinical development programs. Collaborate cross-functionally with clinical development, regulatory affairs, medical affairs, and other teams to ensure alignment and success. Reporting directly ...

Takeda
Lexington, Massachusetts

The Associate Director, Clinical Research provides clinical project management and leadership to ensure successful operational execution of all US Medical Clinical Research including, Medical Affairs Company Sponsored Studies (MACS) collaborative studies and Investigator Initiated Research (IIR). St...

Vertex
Boston, Massachusetts

As the Associate Director of Strategic Sourcing for Cell and Gene Therapy, you will be a part of a fast-growing and innovative organization at the company’s world headquarters in Boston, MA. The Cell and Gene Therapy Sourcing Associate Director is a key leadership role mainly focus on CDMO Sourcing ...

bluebird bio
Somerville, Massachusetts

Our Patient Supply Team is hiring an Associate Director, Supply Chain Planning to be a Business Process Owner for Sales & Operations (S&OP) Planning process and responsible for managing end to end commercial process for cell & gene therapy. Leading and managing a comprehensive Sales and Operations P...

Actalent
Cambridge, Massachusetts

The Clinical Supply Chain Supply Associate supports programs and protocols, in tandem with program leads. He/She manages and maintains IMP distribution and returns drug plans and manages Clinical Supply documentation associated with assigned program, in compliance with GMP and industry standards. If...

State Street
Boston, Massachusetts

Contributing to the formulation and execution of the regulatory strategy by assessing areas of supervisory focus, monitoring the regulatory landscape, and evaluating regulatory intelligence. The Head of Regulatory Interactions is a senior leadership position within State Street’s Corporate Complianc...