Start Date: June 14, 2022 (Summer 2022)

Work Hours: 40 hours per week

Length of Assignment: 3 Months

Education Level & Preferred Majors: PhD, PharmD, ongoing enrollment in an advanced Clinical/Science Degree is preferred (e.g., PharmD, PhD, MSN, MPH, etc.)

Given the current uncertainty of the global pandemic and work from home situation for 2022, this internship is currently planned to be virtual with the option for interns to work remotely from within the U.S. Borders. We will keep candidates informed if this changes.

Due to the ever changing situation concerning the COVID-19 global pandemic, for our summer 2022 internship program we will only consider international candidates who are currently in the US and will remain in the US for the duration of the internship.

Roche's Product Development organization is dedicated to delivering outstanding therapies to patients who need them. We conduct global clinical trials, analyze results, monitor safety, and work with regulatory authorities to provide truly differentiated medicines to patients. This internship will be working in the lymphoma disease area.

Job Description/Responsibilities

Over the span of the internship, the intern would be expected to learn and perform foundational clinical science skills equivalent to a clinical science assistant role. The intern will provide a final presentation (with any topic of relevance/interest in the role, e.g., review of other molecule competitors/competitive landscape, identifying areas of improvement in study conduct, new guidances/criteria applicable to our studies, etc.) at the conclusion of the internship.

Key responsibilities may include, and are not limited to:

• Assist in the review and authorship of key trial related documents including; protocol, informed consent form (ICF), patients narratives, etc.

• Assist with clinical trial data review

• Develop/provide input for clinical presentations including; site initiation visits, investigator meetings, monitoring committees

• Participates in and contributes to study team meetings

• Perform literature reviews

• Assist in strategic project initiatives evaluating different aspects of clinical trial development and report findings

Requirements/Qualifications

• Relevant clinical/scientific experience is preferred

• Proficient computer skills, including Microsoft Office Suite (Word, PowerPoint and Excel)

• Has impeccable ethics.

• Strong attention-to-detail

• Strong project management, organization and time management skills; has a track record of consistently meeting or exceeding assigned goals and objectives

• Strong verbal and written communication skills

• Good influencing and negotiation skills; works well with and through others

• Good judgment and decision-making skills

• Has a demonstrable orientation to team work; has had a successful, previous track record in working effectively and efficiently with cross-functional teams