Quality Control Editor

ProPharma Other US Location

Company

ProPharma

Location

Other US Location

Type

Full Time

Job Description

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

The Quality Control (QC) Editor position is responsible for performing quality reviews and editing of clinical documents, regulatory submissions, medical/ scientific publications, and other related documents.

Essential Functions: 

  • Performs detailed QC review of clinical, nonclinical, and regulatory documents, tables, publications, annual reports, literature summaries, submission sections, internal documents, etc. 
  • Verifies content to ensure accuracy of all factual statements within document text compared to post-text sources cited. 
  • Interprets clinical data and literature as needed to perform QC duties. 
  • Proofreads or substantively edits documents to correct and streamline grammar, spelling, punctuation, style, and format. 
  • Verifies that document content is consistent with internal, client, and related authority guidelines. 
  • Formats, styles, and troubleshoots functionality and presentation of documents and templates. 
  • Ensures compliance of document format per templates and style guides. 
  • Leads resolution of discrepant findings within documents, including documenting actions, verifying implementation of findings, and archiving results. 
  • Possesses knowledge of AMA Manual of Style, other style guides, and any guidelines related to assigned projects. 
  • Supports writers and/or other team members with supportive tasks as requested. 
  • Works cross functionally to continuously improve processes.  
  • Other duties as assigned.  

Necessary Skills and Abilities: 

  • Excellent use of English language. 
  • Expertise in Microsoft Word and understanding of Acrobat/PDF software. 
  • Excellent language skills (reading, writing, editing, team communication). 
  • Pharmaceutical and/or Biotech background strongly preferred. 
  • Exceptional time management skills and attention to detail. 

Educational Requirements: 

  • College degree or 2+ years of education in related field. 

 

Experience Requirements: 

  • At least 3 years of QC/editing-related job history. 

 

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

Apply Now

Date Posted

11/19/2024

Views

0

Back to Job Listings ❤️Add To Job List Company Info View Company Reviews
Positive
Subjectivity Score: 0.8

Similar Jobs

Senior Engineering Manager, Micros Foundations - Atlassian

Views in the last 30 days - 0

Atlassian is seeking a Senior Engineering Manager to lead a team of Backend Software Engineers The role involves guiding technical decisions prioritiz...

View Details

Development Underwriter - Simply Business

Views in the last 30 days - 0

Simply Business is seeking a Development Underwriter with an Underwriting background to support their new MGA brand Nupro which aims to disrupt the sm...

View Details

Senior Software Engineer (Scala/Java) - HERE Technologies

Views in the last 30 days - 0

HERE Technologies is seeking an experienced backend engineer with strong Java or Scala skills to join the Map Processing Pipelines team The role invol...

View Details

Senior Product Analyst - FinCrime Platform - WISE

Views in the last 30 days - 0

Wise is seeking a Senior Product Analyst for its FinCrime Platform The role involves driving analytics efforts in the Financial Crime Platform product...

View Details

Senior Data Analyst - Customer Experience - WISE

Views in the last 30 days - 0

Wise is a global technology company aiming to revolutionize international money transfers by offering minimal fees maximum ease and full speed They ar...

View Details

Lead Data Analyst - Mitigation - WISE

Views in the last 30 days - 0

Wise is a global technology company seeking an Operations Analyst with 4 years of experience in analytics particularly in operational team analytics T...

View Details