Regulatory Medical Writer - Oncology/eCTD Specialist

Integrated Resources Inc.; Collegeville (PA); Presencial; USD 80.000 - 120.000; Tempo integral

Resumo da vaga

Integrated Resources Inc. is seeking a highly organized individual to prepare clinical and regulatory documents. The role demands a scientific/medical background with strong communication skills to effectively convey complex information. Successful candidates will work closely with development teams, managing document production under regulatory guidelines.

Qualificações

• Scientific/medical academic background required with relevant degree.
• Strong functional literacy and experience communicating complex analyses.
• Experience with oncology and eCTD filing preferred.

Responsabilidades

• Prepare clinical regulatory documents and presentations.
• Manage contract writers and ensure consistency in documents.
• Collaborate with cross-functional teams on regulatory issues.

Conhecimentos

Active listening

Analytical skills

Communication

Organization

Formação

MD, DVM, PhD, BSN, PharmD, Master's or Bachelor's in relevant field

Descrição da vaga

Integrated Resources Inc. is seeking a highly organized individual to prepare clinical and regulatory documents. The role demands a scientific/medical background with strong communication skills to effectively convey complex information. Successful candidates will work closely with development teams, managing document production under regulatory guidelines.