Clinical Scientist – FSP

This is a fully remote position, open to applicants in United States.

📋 Description

• Assist the Clinical Study Protocol Lead and the study team in the scientific and clinical execution of clinical studies.

• Provide support for adjudication activities.

• Aid in medical monitoring.

• Prepare reconciliation of imaging data.

• Create materials for meetings.

• Manage deviations from the protocol.

• Support either a single study or multiple studies.

• Lead studies that have a limited scope, such as Survival Follow-up.

• Collaborate with cross-functional teams.

• Engage with both internal and external stakeholders, including study sites and committees, to support clinical study objectives.

• Complete all necessary training curriculum.

• Accurately fill out timesheets.

• Submit expense reports.

• Update CV as necessary.

• Maintain a thorough understanding of and adhere to Parexel processes, ICH-GCPs, and other relevant requirements.

⛳️ Requirements

• Experience in oncology is mandatory.

• Bachelor’s, Master’s, or PhD in Life Sciences with over 2 years of relevant professional experience.

• If lacking a degree in Life Sciences, a Bachelor’s degree along with significant clinical development experience (more than 5 years) is necessary.

• Proven skills in oral and written communication are essential.

• Proficiency in MS Office Suite is required, including Word, Excel, and PowerPoint.

• Advanced skills in Excel are required, particularly with pivot tables and VLOOKUPs.

• Proficient in both written and spoken English.

• Experience in adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and management of protocol deviations.

• Pharmaceutical industry experience is advantageous but not essential.

• A minimum of 2 years of experience in medical monitoring is preferred.

🏝️ Benefits

• Equal opportunity employment.

• Willingness to travel as necessary for important company meetings.