Clinical Research Scientist - Global Trials & Safety

PSG Global Solutions; Summit (NJ); On-site; USD 70,000 - 90,000; Full time

Job summary

A global talent solutions firm in New Jersey is seeking a professional for a key role in medical writing and clinical safety. You will analyze clinical safety data and collaborate with global health authorities. A minimum of 2 years in medical or technical writing is required, along with substantial knowledge of clinical research and drug development processes. Proficiency in Microsoft Office is essential. This position provides significant opportunities for career growth and development.

Qualifications

• Minimum 2 years experience in medical or technical writing.
• Clinical monitoring experience preferred.
• Extensive knowledge in medical/scientific and clinical research.

Responsibilities

• Assist global clinical development and regulatory teams.
• Analyze clinical safety signal data and inform stakeholders regarding risk strategies.
• Interact with clinical development, medical affairs, and regulatory authorities.

Skills

Medical writing

Clinical monitoring

Medical/scientific knowledge

Knowledge of Medical Terminology

Clinical trial design

Pharmacodynamics and pharmacokinetics

Data review and interpretation

Knowledge of GCP and ICH Guidelines

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

EDC databases

SAS datasets

Job description

A global talent solutions firm in New Jersey is seeking a professional for a key role in medical writing and clinical safety. You will analyze clinical safety data and collaborate with global health authorities. A minimum of 2 years in medical or technical writing is required, along with substantial knowledge of clinical research and drug development processes. Proficiency in Microsoft Office is essential. This position provides significant opportunities for career growth and development.