Director, Nonclinical and Clinical Pharmacology Writing

Hobson Prior; Córdoba; Presencial; EUR 70.000 - 100.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company is seeking a Director of Nonclinical and Clinical Pharmacology Writing to oversee the creation of regulatory documents and ensure compliance with guidelines. This role involves mentoring team members and leading writing activities across various programs. Ideal candidates will possess strong communication skills and experience in global regulatory submissions.

Formación

• Experience in writing and leading global regulatory submissions.
• Experience managing and training other writers.
• Ethical, responsible, and respectful approach to work.

Responsabilidades

• Lead the planning and creation of regulatory documents.
• Help develop briefing materials and respond to health authority questions.
• Mentor team members to maintain high standards in document production.

Conocimientos

Strong communication skills

Ability to summarize complex information clearly

Knowledge of global regulatory requirements and guidelines

Herramientas

MS Office

Descripción del empleo

Looking for your next challenge as Director of Nonclinical and Clinical Pharmacology Writing? Our client is a leading pharmaceutical company looking for their next perfect hire!

Hobson Prior is seeking a Director for Nonclinical and Clinical Pharmacology Writing. This role will ensure the timely creation of high-quality documents that support clinical development. You will lead writing activities across various programs with minimal supervision.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities :

• Lead the planning and creation of regulatory documents, including early-stage protocols and summaries for submissions.
• Help develop briefing materials and respond to health authority questions.
• Write and manage documents to ensure they are clear, accurate, and follow guidelines.
• Review and ensure the quality of documents prepared by others.
• Mentor team members to maintain high standards in document production.
• Work with colleagues to ensure compliance with procedures and regulations.

Key Skills and Requirements :

• Experience in writing and leading global regulatory submissions.
• Ability to summarize complex information clearly.
• Strong communication skills and proficiency in MS Office.
• Knowledge of global regulatory requirements and guidelines.
• Experience managing and training other writers.
• Ethical, responsible, and respectful approach to work.

For more information, please contact Indre Semeskeviciute .

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -

J-18808-Ljbffr