Navitas Life Sciences – Job Openings for Trainee Regulatory Associate [Entry-Level]

Explore entry-level pharma jobs in regulatory affairs at Navitas Life Sciences. Join as Trainee Regulatory Associate in Bogota, Colombia—ideal for life sciences graduates seeking global impact in pharmaceutical careers.

About the Company

Navitas Life Sciences, a global tech-driven CRO with over 35 years of expertise, delivers innovative Clinical, Regulatory, Pharmacovigilance, and Data services to pharma and biotech sponsors. Headquartered in Gaithersburg, MD, it ensures regulatory compliance through cutting-edge solutions across 100+ countries, fostering growth and collaboration for life-saving advancements.

Job Details

• Company Name: Navitas Life Sciences
• Experience: Entry Level
• Qualification: Bachelor’s degree in Pharmacy/Pharmaceutical Chemistry, or life sciences related
• Location: Bogota, Colombia
• Work Type: Full Time, On-site

Job Description

Navitas Life Sciences seeks a motivated Trainee Regulatory Associate to support global submissions in its expanding Regulatory Affairs team. This entry-level role in pharma jobs focuses on eCTD publishing and compliance. Gain hands-on experience in life sciences careers while contributing to IND/NDA/MAA applications worldwide.

Trainee Regulatory Associate

• Department: Regulatory Affairs
• Role: Trainee Regulatory Associate
• Experience: Entry Level
• Education/Qualification: Bachelor’s degree in Pharmacy/Pharmaceutical Chemistry, or life sciences related

Skills/Qualifications

• Proficiency in MS Word, MS Excel, MS Access, MS PowerPoint, and Adobe Professional
• Strong understanding of eCTD, NeES/eSub, and paper submission formats
• Knowledge of global agency standards and regulatory procedures
• Excellent troubleshooting skills for document issues in Acrobat and Word
• Ability to perform quality checks and data entry with attention to detail
• Collaborative mindset for cross-departmental planning and stakeholder communication
• Commitment to GMP and quality control for regulatory compliance

Key Responsibilities

• Manage end-to-end publishing for IND/NDA/MAA submissions
• Collaborate on preparation, formatting, and QC of documents
• Support eCTD and global agency submissions with hyperlinking
• Troubleshoot issues and escalate gaps to stakeholders
• Perform validation checks to avoid errors pre-filing
• Train colleagues using train-the-trainer model
• Handle data entry, SharePoint updates, and ancillary requests
• Project manage multiple deadlines with real-time tracking

Benefits/Perks

• Accelerated career growth in a leading CRO environment
• Ongoing learning through on-the-job training programs
• Competitive entry-level salary with performance bonuses
• Inclusive work culture promoting innovation and teamwork
• Global exposure via international projects and collaborations

How to Apply

Visit the Navitas Life Sciences careers portal at https://www.navitaslifesciences.com/opportunities and search for “Trainee Regulatory Associate” in Bogota. Click “Apply” to submit your resume and details.

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Why You Should Join

At Navitas Life Sciences, embrace a culture of innovation and recognition where entry-level talent thrives amid regulatory excellence. Secure long-term stability in a compliant, tech-forward setting that accelerates drug development globally.

Benefit from mentorship, skill enhancement, and diverse projects that empower you to make meaningful healthcare impacts.

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