Clinical Research Scientist - Motion Recruitment : Job Details

A multinational corporation that develops pharmaceuticals and medical technologies is actively seeking a self-motivated Scientist 3- Clinical Research to join their dynamic team. It is a 4-month contract role, Monday through Friday, in their Titusville, New Jersey location.

Come work for a company where the working culture is supportive and the opportunity for growth and development is endless. As Scientist 3, you will be responsible for the translation and implementation of (non-medical) scientific concepts into the study design and/or program across planning, execution, and reporting, including integration of biomarkers, digital technologies, data science initiatives, and select vendors.

Required Skills & Experience

• PhD in relevant field (e.g. Neuroscience, Biomedical Sciences, Biology; chemistry: pharmacy) OR
• PharmD or MD degree from an accredited institution with 1-2 yrs work experience OR
• Masters in relevant field with 2-4 yrs work experience

What You Will Be Doing

Daily Responsibilities

• Responsible for leading the translation of scientific concepts into program and study design.
• Responsible for identifying and implementing (non-medical) scientific aspects of the program and/or study at planning, execution and reporting, including (but not limited to) integration of Biomarkers and Data Science/Digital Health initiatives into studies.
• Oversees the assessment, selection and operational implementation for biomarkers, digital and other endpoints (scales), imaging.
• Accountable for shaping and implementing compound and program DEI strategy together with Clinical Leader.
• Contributes to the preparation of PED, study protocols and training materials for clinical studies.
• Along with SRP or Clinical Leader and global development partners, responsible for oversight and high-quality implementation and closure of the study, ensuring data integrity.
• In concert with operational staff, acts as a liaison between the company and clinical investigators for overarching scientific guidance and other potential non-medical aspects.
• Partners with Regulatory Affairs in developing regulatory strategy and determining requirement for health authority reporting or corrective actions on trial/program level.
• Oversees the set-up of medical review tools to meet medical review plan requirements.
• Contributes in all areas where scientific data will be generated and shared with the patients and/or the scientific community.

Applicants must be currently authorized to work in the US on a full-time basis now and in the future.