Clinical Data Management Early Oncology Internship - Boise, United States - Idaho State Job Bank

Description

Clinical Data Management Early Oncology Internship

• Summer at Takeda Pharmaceuticals in Boise, Idaho, United States Job Description By clicking the 'Apply' button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use .

I further attest that all information I submit in my employment application is true to the best of my knowledge.


Job Description About the role:
At Takeda, we are committed to lifelong learning. To that end, Takeda's summer internship program blends real world experience with an extensive overview of the pharmaceutical industry. Knowledgeable mentors will provide guidance as you gain professional hands-on experience.

The summer internship program is a full-time commitment of 12 weeks and offers a unique perspective into a world-class pharmaceutical company.

Our internship program provides you with the opportunity to network with people at Takeda through various planned events and activities.

Please note that Takeda does not provide intern housing or a housing stipend. This position will be remote.


How you will contribute:
+ Exceptional interpersonal, verbal communication and writing skills. + Deadline-driven with an elevated level of organizational and planning skills. + Strong quantitative, analytical, problem solving and conceptual skills. + Proven record of accomplishment of teamwork, adaptability, innovation, initiative, and integrity. + Global mindset to grow in a diverse work environment. + Work with Clinical Data Management (CDM) to develop standard data review expectations and associated documentation for sensitive, specialized external data. + Work with CDM, including CDM Operations, to integrate novel data flows into existing ways of working and identify necessary enhancements/changes to processes/resource materials/trainings/technologies. + Work with CDM to conduct/coordinate data review using these pilot materials in select clinical trials. + Leveraging existing materials, work with the team and vendors (as applicable) to develop new training or resource materials for CDM team members for sensitive, specialized external data.


Requirements / Qualifications:
+ Currently authorized to work in the US (United States) without sponsorship. Takeda does not provide sponsorship for internship positions. + Available to work full-time (40 hours/week), within the core business hours of 8:00am - 5:00pm, for 12 weeks during the summer months. + Undergraduate, Graduate, PhD, MD s To view full details and how to apply, please login or create a Job Seeker account