Clinical Research Scientist Intern

Genmab•Plainsboro Township, NJ

40d•Hybrid

About The Position

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so. Does this inspire you and feel like a fit? Then we would love to have you join us! Why Genmab Our internship program provides interns with hands-on experience and relevant projects that directly align with our company’s goals. Additionally, we believe our program provides a valuable opportunity to learn, thrive, and build a strong network. We encourage you to review our website to learn why we’re always looking for smart, purpose-led candidates to play a role in our bold, extra[not]ordinary® future. Job Overview The Clinical Research Scientist (CRS) Intern supports Genmab’s drug development efforts by gaining hands-on experience in clinical research science within the Clinical Strategy Team (CST) during a 10-week summer internship. This internship offers exposure to the role of clinical scientist and oncology clinical trials through practical assignments and mentorship. The intern will work closely with other CST members, as well as within cross-functional teams, contributing to ongoing clinical trial-related activities in order to provide high-quality and timely deliverables.

Requirements

Candidate for PhD, Pharm D, MS or BS degree within the medical, biological, pharmaceutical science or related discipline
Basic understanding of clinical research
Strong analytical and problem-solving abilities.
Excellent written and verbal communication skills.
Ability to work independently and as part of a collaborative team.
High attention to detail and commitment to quality work.
Genuine interest in clinical research and drug development.

Nice To Haves

Demonstrates initiative, a proactive attitude, and eagerness to learn in a fast-paced environment.
Effectively communicates and collaborates with team members, mentors, and stakeholders.
Maintains attention to detail and quality in all deliverables while managing multiple tasks.
Actively engages with CRS team members while leveraging their feedback

Responsibilities

Works in collaboration with other Clinical Research Scientists
Assists in supporting CRS team members in executing the clinical trial in alignment with the clinical development plan (CDP)
May assist Sr. level CRS with the development of a trial protocol and to other study-related documents
Exposure and education on performing ongoing data review, and summarizing efficacy and safety data for interpretation/analysis
Participate in mentorship meetings and contribute to team discussions on process improvements and best practices.
Provide general administrative support to the Global CRS team.
Assist with the organization and planning of relevant team meetings for the Global CRS Team, and CRS leaders including generating agendas, meeting logistics, developing meeting minutes/action items and archiving.
Assist with internal coordination of activities related to the CRS role in support of clinical trials.
Provide support with the oversight and maintenance of Global CRS Team folder structure and coordination with relevant stakeholders.
Assist with tracking progress across multiple initiatives, workstreams, and programs including communication to CRS and internal stakeholders as requested.
Assist with the management and filing of medical-responsible regulatory documents in the eTMF adhering to required indexing administration with routine review for clinical trial completeness.
Provide support for inspection readiness by contributing to the establishment, tracking, maintenance, and quality control of the medical-responsible regulatory documents in the eTMF.
Conduct scientific research for publication or indication searches.
Create, edit and quality check word documents, templates, PowerPoint presentations, and Excel worksheets.
Ad-hoc task/projects as assigned.