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.***
Top Skills
What We Do
ProPharma is the premier Research Consulting Organization (RCO), delivering fully customizable consulting solutions to empower biotech, med device, and pharmaceutical organizations of all sizes to advance scientific breakthroughs confidently and introduce new therapies.
With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risk and accelerate high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science
