Oncology Research Scientist Intern - Beerse, België - Johnson & Johnson

Johnson & Johnson

Geverifieerd bedrijf

Beerse, België

1 week geleden

Geplaatst door:

Sophie Dubois

beBee Recruiter

Beschrijving

At Johnson & Johnson, we use technology and the power of teamwork to discover new ways to prevent and overcome the world's the most significant healthcare challenges.

Our Corporate, Consumer Health, Medical Devices, and Pharmaceutical teams leverage data, real-world insights, and creative minds to make life-changing healthcare products and medicines.

We're disrupting outdated healthcare ecosystems and infusing them with transformative ideas to help people thrive throughout every stage of their lives.

With a reach of more than a billion people every day, there's no limit to the impact you can make here.

Are you ready to reimagine healthcare?

Here, your career breakthroughs will change the future of health, in all the best ways. And you'll change, too.

You'll be inspired, and you'll inspire people across the world to change how they care for themselves and those they love.

Amplify your impact. Join us

The Clinical Scientist intern may contribute to Cross-Functional Trial Team (CFTT) activities, including but not limited to developing the clinical trial protocol, clinical trial materials, literature searches and review, medical review of trial data, coordinating completion of clinical study reports and providing support (as needed) for preparation of relevant documents for regulatory filings.

The intern may also collaborate with the Study Responsible Scientist (SRS), the Study Responsible Physician (SRP), and or other project teams in various functional disciplines in monitoring and or supporting various aspects of clinical trial conduct.

Each intern will have their own or group assigned projects and will be expected to present their work to their project teams, the oncology Senior Leadership Team (SLT), and as a poster/abstract at the research symposium at the end of the internship.

Responsibilities may include:

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)
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 crossfunctional team and clinical team meetings
Development of study training materials/documents
Shadowing key clinical and or functional roles for learning/development opportunities
Observing Site Initiation Visits (SIVs)
Supporting Clinical Team with study start up activities during trial set up, and other study tasks during conduct, and close out
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
Review of medical literature, related products, and new technologies
Collaboration and or assigned projects from other various functional disciplines
Leadership opportunities on specific program and or group projects
Abstract/poster preparation and presentation at organizationwide research symposium
Other projects as assigned

Qualifications:

Qualifications:

Undergraduate college students with completion of a minimum of four semesters
Currently enrolled in a biology, chemistry, premed, or nursing program
Graduate students must be pursuing a master's, PharmD or PhD degree
Fluent in written and spoken English
Good verbal and written communication skills
Good presentation skills; leading presentations to peers, project teams and senior leadership teams
Working knowledge and or experience using key Microsoft suite of business tools including but not limited to Outlook, Excel, PowerPoint, Word, Teams, Slack, SharePoint, OneNote, etc.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.