Clinical Scientist – FSP

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

📋 Description

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

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

• Support one or several studies simultaneously.

• Lead a focused-scope study, such as Survival Follow-up.

• Collaborate with cross-functional teams.

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

• Complete the mandatory training curriculum.

• Accurately fill out timesheets.

• Submit expense reports as needed.

• Update your CV as necessary.

• Stay informed about and adhere to Parexel processes, ICH-GCPs, and relevant regulations.

⛳️ Requirements

• Proven oral and written communication abilities.

• Experience with MS Office Suite is essential, including Word, Excel, and PowerPoint.

• Proficient in both written and spoken English.

• Proficient in the local language, if applicable.

• Willingness to travel as needed for important company meetings.

• Experience in the pharmaceutical industry is advantageous but not mandatory.

• Experience in specific therapeutic areas is a plus.

• Preferably, 2 years of experience in medical monitoring.

• Bachelor's, Master's, or PhD in Life Sciences with a minimum of 2 years of relevant work experience.

• If lacking a degree in Life Sciences, substantial experience in clinical development (over 5 years) is required.

🏝️ Benefits

• Equal opportunity employer.

• Willingness to travel as required for key company meetings.