Senior Director Executive Director Medical Writing

The Senior Director / Executive Director Medical Writing is a senior management position member of the Senior Leadership Team; Acts as Head of PV Medical Writing Group and has primary responsibility to ensure the contracted PV activities are appropriately performed in line with company policies/procedures and in compliance with global regulations. 

Responsibilities

• Lead the PV Medical Writing function ensuring high-quality compliant and timely deliverables.
• Manage and develop the PV Medical Writing team fostering performance engagement and professional growth.
• Drive quality compliance inspection readiness and continuous improvement initiatives including oversight of SOPs KPIs audits and regulatory inspections.
• Provide strategic PV medical writing expertise and subject matter leadership to clients internal stakeholders and project teams.
• Support business development activities including proposals bid defenses and client engagements.
• Oversee departmental resources budgets and operational performance to ensure efficient service delivery.
• Review regulatory safety responses and contribute to Risk Management Plans aggregate reports and other key pharmacovigilance deliverables.
• Build and maintain strong client relationships ensuring exceptional service and trusted partnerships.
• Represent the organization externally through industry engagement publications presentations and professional development activities.

Qualifications :

The preferred candidate will have:

• Extensive pharmacovigilance and PV Medical Writing experience including leadership and people management of high-performing teams.
• Deep knowledge of global pharmacovigilance regulations with expertise in authoring and reviewing aggregate safety reports and PV procedures.
• Proven experience supporting regulatory compliance inspections and pharmacovigilance system oversight including QPPV or Deputy QPPV responsibilities.
• Strong business acumen with experience supporting proposals client engagements and bid defense activities.
• Excellent scientific regulatory and analytical capabilities including translating complex clinical and safety data into clear high-quality regulatory and scientific documents

Additional Information :

When you join Ergomed Group you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. Youll join a passionate and collaborative team of experts in clinical research pharmacovigilance and quality consulting.

We are diverse in many ways yet our values unite us. Our values are how we work not words on a wall. If they sound like you you will feel at home here.

• Quality: we hold ourselves to the standard patients deserve.
• Integrity and trust: we do the right thing especially when it is hard.
• Drive and passion: we care about the outcome because someone is waiting on it.
• Agility and responsiveness: we move quickly because patients cannot wait.
• Belonging: everyone is welcome and every voice counts.
• Collaborative partnerships: we go further by going together.

We look forward to welcoming your application.

Remote Work :

Yes

Employment Type :

Full-time