Oncology clinical scientist intern

• Gaining overall understanding of clinical research and drug development including but not limited to Good Clinical Practices (GCPs), International Conference of Harmony (ICH) guidelines, and Standard Operating Procedures (SOPs)
• Attend “Bench to Bedside” Lecture Series to gain knowledge of the drug development process and clinical research
• Assisting with management of trial activities including patient tracking through screening process, and eligibility/enrollment reviews
• Assisting with document processing and management within the electronic master file (i.e., vTMF)
• Participating in department and team meetings
• Participating in cross-functional team and clinical team meetings
• Developing study training materials/documents
• Shadowing key clinical and or functional roles for learning/development opportunities
• Observing Site Initiation Visit (SIV) Meetings (if applicable for assigned projects)
• Supporting Clinical Team with study start up activities during trial set up, and other study tasks during conduct, and close out (depending on the stage of the trial)
• Assisting with review and cleaning of clinical data (i.e., medical review), query generation and resolution
• Assisting with interpretation, reporting, and preparation of oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissions (if applicable)
• Reviewing medical literature, related products, and new technologies
• Providing necessary training to local operational teams
• Collaboration with and/or assigned projects from other various functional disciplines
• Leadership opportunities on specific program activities and/or group projects
• Abstract/poster preparation and presentation at organization-wide annual research symposium
• Other projects as assigned

• Legally/permanently authorized to work in Belgium with no required sponsorships
• Must be currently enrolled in an accredited University or College program throughout the duration of the internship
• Must not be graduating before, during, or after the start or end of the internship program
• Currently enrolled in biology, cell/molecular biology, chemistry, pre-med, nursing program, public health, biochemistry, biomedical engineering, oncology, clinical pharmacology, clinical or translational research, computational biology, precision medicine, or similar areas of study
• Undergraduate students with completion of a minimum of four semesters at program start or graduate students are eligible
• Minimum cumulative GPA of 3.0
• Students in good standing, working towards the completion of an undergraduate or graduate degrees
• Graduate students must be pursuing a master’s, PharmD, Physician Assistant or PhD or other clinical related degrees
• Self-motivated, future scientist leaders passionate about drug development and clinical research
• Detailed oriented with good organizational skills
• Possess strong leadership skills to participate and contribute to internship program initiatives and events
• Fluent in written and spoken English
• Great interpersonal, verbal and written communication and presentation skills
• Ability to lead peers, project teams and present to project and senior leadership teams
• Enthusiastic, collaborative, able to build relationships and work within global matrixed and cross-functional teams
• Ability to work on and balance multiple project deliverables
• Working knowledge and/or experience using Slack, Microsoft suite of business applications/tools including but not limited to Excel, OneNote, Outlook, PowerPoint, Sharepoint, Teams, and Word

Proven leadership/participation with campus programs and/or service programs is desired

We offer an inclusive work culture that is open, innovative, and performance driven