Life Sciences Job at IQVIA | Apply Now
Looking for a promising life sciences job in the clinical research field? IQVIA is hiring a Regulatory Maintenance Associate for clinical trials in Mexico City. This role offers an excellent opportunity for candidates with regulatory experience to work on global submissions, support clinical trials, and grow within one of the leading organizations in healthcare intelligence.
- Job Position: Regulatory Maintenance Associate, Clinical Trials
- Location: Mexico City, Mexico
- Job ID: R1541438
About the Company
Life Sciences Job seekers looking for global exposure will find IQVIA an ideal choice. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company focuses on accelerating the development and commercialization of innovative medical treatments to improve patient outcomes worldwide. With a strong reputation in iqvia careers, it continues to be a top destination for professionals exploring jobs in Mexico and beyond.
Job Description
Life Sciences Job responsibilities include preparing and reviewing regulatory documents to support clinical trial submissions. The role involves providing regulatory support for complex projects under senior guidance while independently managing straightforward assignments.
The candidate will act as a Clinical Trial Regulatory Manager (CTRM) for simpler projects and assist in complex regulatory submissions. Responsibilities also include reviewing scientific documentation, conducting gap analysis, and maintaining submission dossiers in compliance with regulatory standards.
You will collaborate with internal and external stakeholders, provide strategic regulatory input, and support global submissions, including European centralized submissions. Ensuring quality deliverables, meeting timelines, and adhering to SOPs and project plans are key aspects of this iqvia careers opportunity in jobs in Mexico.
Qualifications
Life Sciences Job applicants must hold:
- Bachelor’s Degree in Life Sciences or related discipline
- 1–2 years of experience with EU CTIS and global core pack knowledge
- Experience in country oversight, especially for amendments
- Understanding of R&D processes (CMC, Preclinical, Clinical)
- Knowledge of regulatory laws and guidelines
- Proficiency in Microsoft Office, CTMS, SA WF, SAFE, Wingspan
- Strong interpersonal and communication skills (written and oral)
- Good organizational and time management skills
- Ability to build effective working relationships
- Self-motivated with strong enthusiasm
- Ability to handle multiple projects simultaneously
- Strong adherence to SOPs with process improvement mindset
- Ability to make decisions under senior supervision
Key Responsibilities
Life Sciences Job duties include:
- Prepare and review regulatory documents for clinical trial submissions
- Act as Clinical Trial Regulatory Manager (CTRM) on straightforward projects
- Support complex regulatory projects under senior guidance
- Perform scientific documentation review and gap analysis
- Maintain clinical trial submission dossiers as per regulatory requirements
- Provide regulatory guidance to internal and external stakeholders
- Support European centralized and global submissions
- Ensure timely delivery of high-quality regulatory outputs
- Maintain internal systems, databases, and tracking tools
- Participate in audits related to projects and systems
- Understand project scope, deliverables, and timelines
