Remote Medical Writer — Clinical Docs & Regulatory

Ladders; United States; Remote; USD 100.000 - 120.000; Vollzeit

Benefits dieser Stelle

National medical, dental, and vision  

Tuition reimbursement

Paid time off and holidays

Parental leave and caregiver leave

401(k) and employee stock purchase

Zusammenfassung

Ladders is seeking a Medical Writer - Medical Information to join a leader in Pharmaceuticals & Biotech. This remote role focuses on developing high-quality scientific and clinical documentation that supports medical information activities across the drug development lifecycle.

The position will partner closely with program management and cross-functional teams to keep deliverables on track, ensure documentation quality, and support timely submissions in a highly compliant environment.

Qualifikationen

• Bachelor's degree in a scientific discipline or equivalent.
• At least 2 years of relevant experience in medical writing or a related field.
• Experience in the pharmaceutical or CRO industry preferred.
• Familiarity with scientific writing and regulatory documentation.
• Strong command of English grammar, editorial, and proofreading skills.

Aufgaben

• Write and provide input on clinical documents such as reports and protocols.
• Assist with complex clinical documents including IBs, INDs, and MAAs.
• Ensure compliance with quality processes for assigned documents.
• Support program management by developing timelines and forecasts.
• Represent the medical writing function in meetings.

Kenntnisse

Editorial skills

English grammar

Regulatory writing

Ausbildung

Bachelor's degree in a scientific discipline

Jobbeschreibung

Ladders is seeking a Medical Writer - Medical Information to join a leader in Pharmaceuticals & Biotech. This remote role focuses on developing high-quality scientific and clinical documentation that supports medical information activities across the drug development lifecycle.

The position will partner closely with program management and cross-functional teams to keep deliverables on track, ensure documentation quality, and support timely submissions in a highly compliant environment.