Senior Clinical Research Scientist

Genmab

Copenhagen or Remote, Denmark

You will as a Senior CRS be part of the Medical department and responsible to contribute to the implementation of the global development strategy, leading or co-leading one or more clinical trials in a therapeutic area for one or more compounds in various stages of clinical development. This may include clinical trial implementation, and oversight of all aspects of clinical development working closely with the Medical Director and other cross-functions to provide high-quality and timely deliverables.

Key Responsibilities Include

Lead or co-lead one or more clinical trial(s) in a therapeutic area for one or more compounds.
Work closely with Medical Director and other Sr. level Clinical Research Scientist (as warranted).
Contribute to the development of the program strategy for assigned trials/compounds and participate in the development of the clinical development plan (CDP) .
In collaboration with the Medical Director, contribute to the development of clinical and regulatory documents, annual safety updates, and registration dossiers (i.e., protocol, ICF, IB, annual safety updates, study reports, regulatory submissions [Briefing documents, IND, Clinical dossiers] to support registration and commercialization of the compound(s).
Participate in the development of case report forms (eCRFs), eCRFs completion guidelines, and provide scientific support for other key data management deliverables (e.g. database lock activities).
Lead the development of the medical data review plan (MDRP), perform ongoing data review, and summarize efficacy and safety data for interpretation/analysis.
Contribute medical input for country/site selection, feasibility assessment and engage in KOL interaction.
Prepare charters and coordinate internal/external committee meetings including presentation preparation (ie, Dose Escalation Committee, DMC, Steering Committee, and Safety Committees).
Participate in the development and review of study plans and serve as a liaison to project teams and CROs.
Provide input for the development of publications in coordination with Scientific Communications.
Contribute to training at Investigator meetings, CRO/CRA training, SIVs as warranted.

Requirements

PhD, Pharmacy, Master in Science or equivalent preferably within the medical, biological, pharmaceutical science or related discipline.
Minimum of 6 years of experience in clinical research with at least 3 or more years of drug development experience.
Prior oncology/hematology drug development experience is a plus.
Proven skills from working in a project oriented matrixed team environment.

About You

You are passionate about our purpose and genuinely care about our mission to transform the lives of patients through innovative cancer treatment.
You bring rigor and excellence to all that you do. You are a fierce believer in our rooted-in-science approach to problem-solving.
You are a generous collaborator who can work in teams with diverse backgrounds.
You are determined to do and be your best and take pride in enabling the best work of others on the team.
You are not afraid to grapple with the unknown and be innovative.
You have experience working in a fast-growing, dynamic company (or a strong desire to).
You work hard and are not afraid to have a little fun while you do so.

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