Senior Regulatory Writing Specialist at Med Communications
Remote, Oregon, USA -
Full Time


Start Date

Immediate

Expiry Date

26 Nov, 25

Salary

0.0

Posted On

26 Aug, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Powerpoint, Stressful Situations, Microsoft Word, Conflict, Spoken Word, Pharmaceutical Industry, Consideration, Training, Mastery, Excel, Commitments, Life Sciences, Writing, Computer Skills, Medicine, Time Management, Teamwork, Outlook, Regulatory Guidelines

Industry

Pharmaceuticals

Description

COVER LETTER REQUIREMENT

We encourage applicants to include a cover letter outlining their interest in the position and relevant qualifications and experiences.

POSITION SUMMARY

The Senior Regulatory Writing Specialist is a professional responsible for the creation of regulatory materials for investigational and marketed products in alignment with regulatory and compliance practices. The individual will work directly with client teams to manage regulatory writing projects.

POSITION QUALIFICATIONS

  • Above average attention to detail, teamwork and initiative.
  • Ability to interact with other departments within the company and be proficient in written and verbal communication.
  • Proficient in Microsoft Word, Excel, Power Point, and Outlook, and quickly able to learn new software.
  • Ability to apply regulatory guidelines to content development.

Competency Statements

  • Ethical - Ability to conform to a set of values and accepted standards.
  • Accountability - Ability to accept responsibility and account for his/her actions.
  • Accuracy - Ability to perform work accurately and thoroughly.
  • Analytical Skills - Ability to use thinking and reasoning to solve a problem.
  • Detail-Oriented - Ability to pay attention to the minute details of a project or task.
  • Self -Motivated - Ability to be internally inspired to perform a task to the best of one’s ability using his or her own drive or initiative.
  • Organized - Possesses the trait of being well organized or following a systematic method of performing a task.
  • Tactful - Ability to show consideration for and maintain good relations with others.
  • Problem Solving - Ability to find a solution for or to deal proactively with work-related problems.
  • Project Management – Ability to develop and complete a project in a timely manner.
  • Active Listening - Ability to actively attend to, convey, and understand the comments and questions of others.
  • Customer-Oriented - Ability to take care of client needs while following company procedures.
  • Communication, Written - Ability to communicate clearly and concisely in writing.
  • Communication, Oral - Ability to communicate effectively and professionally with others using the spoken word. Ability to present information to clients via in-person, videoconference, or phone presentations.
  • Applied Learning - Ability to participate in needed learning activities in a way that makes the most of the learning experience.
  • Working Under Pressure - Ability to complete assigned tasks under stressful situations.
  • Regulatory Understanding – Ability to apply regulatory and compliance guidelines to pharmaceutical industry.
  • Time Management - Uses time effectively and productively, prioritizes tasks, delivers results on time, solves problems quickly and decisively.
  • Work Ethic - Highly motivated, produces consistent high-quality work, has a desire to work hard, takes responsibility, learns from mistakes, follows through with commitments, is professional, is inclusive and welcoming, has respect for others, and goes above and beyond what is required.
  • Behavior and Attitude - Treats others with respect, projects and promotes a positive attitude, uses appropriate behavior, establishes good working relationships, resolves conflict effectively, and speaks kindly to others.
  • Self-Motivated - Ability to be internally inspired to perform a task to the best of one’s ability using his or her own drive or initiative.

SKILLS AND ABILITIES

Education: Advanced degree in a scientific discipline (eg, life sciences, pharmacy, medicine) or relevant work experience; or equivalent combination of education, training, and experience.
Experience: More than 2 years (typically 3-5 years) of experience in scientific/medical/regulatory writing in the pharmaceutical domain. Mastery of 3 or more regulatory document types.
Computer Skills: Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook

How To Apply:

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Responsibilities

To accomplish this job successfully, an individual must be able to perform, with or without reasonable accommodation, each essential function satisfactorily. Reasonable accommodation may be made to help enable qualified individuals with disabilities to perform the essential functions.

Essential Functions Statements

  • Serve as lead writer on regulatory documents (e.g., protocols, CSRs, briefing books, INDs, NDAs).
  • Manage timelines and communications for at least three concurrent writing projects.
  • Organize and lead document review meetings with cross-functional teams, clarify and incorporate feedback, work with cross-functional subject matter experts to resolve unclear comments and differences of opinion between functional areas.
  • Ensure clarity, consistency, and accuracy across all assigned deliverables.
  • Perform document-level quality control review (including abbreviations, references to sources, data in text versus data in tables, figures, or graphs, etc.) and contribute to peer reviews (logical flow, sense check etc.).
  • Collaborate with subject matter experts to resolve feedback and align messaging.
  • Contribute to writing process improvements, SOP development, and best practices documentation.
  • Support training or mentoring of less experienced writers on specific document types.
  • Develops project-level lexicons and conventions.
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