Clinical Operations Scientist: Study Design & Trials

Scorpion Therapeutics; Rahway (NJ); On-site; USD 60,000 - 90,000; Full time

Job summary

Scorpion Therapeutics seeks a clinical research professional to perform medical monitoring and support across studies, with responsibilities spanning protocol development, materials preparation, and vendor deliverables. You will interact with stakeholders to ensure data integrity and trial success.

The role emphasizes cross-functional collaboration, medical writing, and adherence to regulatory requirements within a pharmaceutical development context.

Qualifications

• Bachelor’s degree + 2 years OR Master’s + 1 year pharma/clinical development experience.
• Life sciences degree preferred.
• Experience in clinical study design and regulatory writing is valued.

Responsibilities

• Responsible for clinical/scientific activities on a single study or across multiple studies as delegated.
• Support development of study protocols and related materials.
• Interact with internal and external stakeholders in support of study objectives.
• Support development of site and CRA training materials.
• Prepare clinical narratives for eDMC meetings or submissions.
• Collaborate to monitor/track study data, deliverables, and supplies.
• Contribute to design of vendor deliverables aligned with the protocol.
• Support evaluation and tracking of protocol deviations and trends.

Skills

Clinical Research

Clinical Sciences

Clinical Study Design

Clinical Trials Operations

Medical Writing

Protocol Writing

Regulatory Writing

Trial Design

Education

Bachelor’s degree + 2 years

Master’s + 1 year

Job description

Scorpion Therapeutics seeks a clinical research professional to perform medical monitoring and support across studies, with responsibilities spanning protocol development, materials preparation, and vendor deliverables. You will interact with stakeholders to ensure data integrity and trial success.

The role emphasizes cross-functional collaboration, medical writing, and adherence to regulatory requirements within a pharmaceutical development context.