Clinical Content QC Editor

Freyr Solutions; Colombia; Remote; COP 36.310.395 - 59.004.392; Vollzeit

Benefits dieser Stelle

Competitive salary and benefits package

Flexible work environment (remote or hybrid options)

Continuous professional growth through training and development

Inclusive, collaborative, and innovative work culture

Zusammenfassung

A leading global Regulatory Solutions company is seeking a Clinical Content QC Editor in Bogota, Colombia. The role involves comprehensive quality control of clinical regulatory documents, ensuring accuracy and compliance. Join a dynamic team that values innovation and collaboration while enjoying a flexible work environment and opportunities for professional growth.

Qualifikationen

• Comprehensive QC review of clinical sections of regulatory documents.
• Verification of internal consistency within a document.
• Checking of data presented in text and tables/figures against source documents.

Aufgaben

• Documentation of QC findings in the appropriate manner/tool.
• Review for grammar, punctuation, spelling and compliance with specified styles/standards.
• Maintenance of the QC records and checklists.

Jobbeschreibung

Direct message the job poster from Freyr Solutions

Global Talent Acquisition Manager | Specializing in Pharma/Bio-Tech/Med and IT | Experienced in lifecycle recruitment across the Americas and…

About Freyr

Freyr is a leading global Regulatory Solutions and Services company, supporting large, mid, and small-sized global Life Sciences companies. With a mission to accelerate compliance and enable businesses to bring their products to market faster, Freyr operates in a dynamic, innovative, and collaborative environment. Our team of experts works on cutting-edge projects that drive meaningful impact across pharmaceuticals, biotechnology, cosmetics, food, and medical devices industries.

At Freyr, we believe in fostering talent and creating an inclusive work culture where employees are empowered to succeed. Join a company that values innovation, integrity, and the power of collaboration.

Job Title: Clinical Content QC Editor

Location: Bogota, Colombia (Remote)

Job Type: Permanent

Job Description

• Comprehensive QC review of clinical sections of regulatory documents, including but not limited to, IBs, Investigational New Drug (IND) applications, New Drug Applications (NDAs), Biologic License Applications (BLAs), Clinical Trial Applications (CTAs), Marketing Authorization Applications (MAAs), briefing packages for regulatory agency meetings/advice, including verification of all references and source data, to achieve the highest quality from a technical, regulatory, and compliance perspective.
• Verify internal consistency within a document and across related documents.
• Comprehensive content QC of clinical data/reports.
• Documentation of QC findings in the appropriate manner/ tool
• Content QC activity is applicable for all therapeutic areas, development phases, modalities and geographic regions.
• Checking of data presented in text and tables/figures against source documents for consistency and accuracy.
• Verification of the data/content (100%) including text, tables, and figure as per the source documents.
• Review for grammar, punctuation, spelling and compliance with specified styles/standards.
• Maintenance of the QC records and checklists.

What We Offer:

Competitive salary and benefits package.

Flexible work environment (remote or hybrid options available).

Opportunity to work with a global team and contribute to impactful projects.

Continuous professional growth through training and development programs.

Inclusive, collaborative, and innovative work culture.

Why Join Freyr:

Be part of a global, fast-growing organization that operates in over 150 countries.

Opportunity to work on impactful projects in a dynamic and innovative environment.

Competitive salary and benefits package, including performance-based incentives.

Flexible work options to support work-life balance.

Continuous learning and professional development opportunities.

Collaborative and inclusive work culture that values diversity.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Writing/Editing, and Quality Assurance

• Industries

  Research Services, Biotechnology Research, and Pharmaceutical Manufacturing

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