Remote opportunity at
ErgomedMedical Writer III (Pharmacovigilance)
Ergomed is looking for a Medical Writer III specializing in pharmacovigilance to join its expanding medical writing team. The person in this role will handle regulatory…
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About This Role
Ergomed is looking for a Medical Writer III specializing in pharmacovigilance to join its expanding medical writing team. The person in this role will handle regulatory documentation, partner with clients, and help mentor less experienced staff members. This position is remote and suits a detail-oriented professional with a regulatory writing background. Ergomed Group operates in clinical research, pharmacovigilance, and quality consulting. Through its PrimeVigilance division, the company functions as a…
Job Description
Ergomed is looking for a Medical Writer III specializing in pharmacovigilance to join its expanding medical writing team. The person in this role will handle regulatory documentation, partner with clients, and help mentor less experienced staff members. This position is remote and suits a detail-oriented professional with a regulatory writing background.
Ergomed Group operates in clinical research, pharmacovigilance, and quality consulting. Through its PrimeVigilance division, the company functions as a global pharmacovigilance specialist, assisting clients with regulatory frameworks and patient safety from early development to post-marketing surveillance. The organization values quality, integrity, drive, agility, belonging, and collaboration, maintaining a workplace spanning Europe, North America, South America, Asia, and Australia.
Responsibilities
- Write, review, and perform quality checks on regulatory and pharmacovigilance papers such as PSURs, PBRERs, PADERs, ACOs, DSURs, and Risk Management Plans
- Maintain scientific accuracy and regulatory compliance while meeting established deadlines
- Partner with cross-functional groups to analyze, interpret, and present safety data
- Serve as a dependable contact for clients to aid project execution and build working relationships
- Train, mentor, and share knowledge with junior medical writers
- Participate in process improvements and quality enhancement initiatives
Requirements
- Degree in medicine, pharmacy, or a life science discipline
- Minimum of two years of experience in medical writing or related fields including case processing, signal detection, or risk management
- Background ideally gained within a contract research organization environment
- Capability to manage multiple diverse tasks and prioritize duties with close attention to detail
- Proficiency in training and mentoring associate medical writers
- Strong teamwork abilities
- Fluent English language skills
Qualifications
- Master of Science degree
- Doctor of Philosophy degree
- Fluency in an additional language
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
Is this position remote?
Yes, the source posting designates this role as remote.
What is the employment type?
The posting specifies this is a full-time position.
What education is required?
Applicants must hold a degree in medicine, pharmacy, or a life science, with a Master's or PhD noted as desirable.
Does the posting list a salary?
No, the salary is not stated in the source posting.
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