EVERSANA Internship – Hiring in Pharmacovigilance Career as a Safety Analyst (Remote)

EVERSANA is at the forefront of the pharmaceutical and life sciences industry, and we are looking for the next generation of talent. We are excited to offer a remote internship opportunity for a Safety Analyst. This is a unique chance for a motivated individual to gain invaluable experience in the critical field of pharmacovigilance (PV).

About the Role: Safety Analyst (Intern)

This is more than just an internship; it’s a hands-on role where you will be a key contributor to our Pharmacovigilance department. You will support essential safety reporting and data analysis projects, working alongside experienced professionals and making a real impact. Excellent communication skills are a must for this position.

Your Essential Duties and Responsibilities

As a Safety Analyst Intern, you will be integral to our PV operations. Your contributions will be vital in meeting client project deadlines and ensuring regulatory compliance.

Key Responsibilities:

• Aggregate Report Development: Support the drafting and quality control of aggregate safety reports, including PADERs, DSURs, and PSURs/PBRERs.
• Data Analysis and Compilation: Generate project-specific line listings and compile safety data from clinical trials and post-marketing sources.
• Regulatory Compliance: Adhere to safety management plans (SMPs), pharmacovigilance agreements (PVAs), and global regulatory guidelines.
• Stakeholder Collaboration: Work with various internal and external stakeholders to ensure outputs from the safety database meet project needs.
• Operational Support: Provide support for PV operations, including audits and inspections, and assist with other safety writing deliverables as needed.

What We’re Looking For: Ideal Candidate Profile

We are seeking a candidate with a strong foundation in life sciences and a keen interest in drug safety.

Minimum Knowledge, Skills, and Abilities:

• Education: A BS degree in a life science discipline (e.g., pharmacy, nursing) is preferred.
• Knowledge: A broad understanding of domestic and international drug safety regulations and ICH guidelines. Familiarity with clinical trial methodology is a plus.
• Technical Skills: Familiarity with safety databases (e.g., ARGUS, ARISg) and MedDRA is highly beneficial.
• Personal Attributes: Strong attention to detail, a proactive approach, and the ability to work effectively in a team environment. You must be quality-oriented and able to follow established processes.

What is Expected of You

This role comes with real responsibility and the chance to deliver tangible results.

• Client Delight: Your work will directly contribute to client satisfaction and project success.
• Collaboration: You will work collaboratively with the EVERSANA PV team, taking direction and feedback from management and clients.
• Independence: We are looking for someone who can work independently to develop high-quality, scientifically accurate, and compliant medical content.
• Commitment to Diversity: You will be expected to demonstrate a commitment to diversity, equity, and inclusion through your actions and behaviors.

How to Apply

If you are ready to launch your career in pharmacovigilance and gain unparalleled experience in the pharmaceutical industry, we encourage you to apply. This position was originally posted on LinkedIn. To apply, please search for the “Safety Analyst (Intern)” role on the EVERSANA careers page or on LinkedIn.

Verified Internship

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