Contractor - Clinical Research Scientist
Contractor - Clinical Research Scientist
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
At Genmab we are dedicated to building extranotordinary 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!
Sr. Clinical Research Scientist Contractor
Responsibilities
You will be responsible for:
- 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 (e.g. 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
- 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) 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
- Provide medical input for country/site selection feasibility assessment and engage in KOL interaction
- Prepare charters and coordinate internal/external committee meetings including presentation preparation (i.e. 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
- Prepare presentations for Investigator meetings CRO/CRA training SIVs as warranted
- Mentor junior level Clinical Research Scientists as required
Requirements
Moreover you meet the following professional requirements:
- PhD Pharm D MS or equivalent degree preferably within the medical biological pharmaceutical science or related discipline
- Minimum requirement: 6 years of experience in clinical research with at least 3 or more years of drug development experience (preferably inoncology/hematology)
- Experience working in a project-oriented matrixed team environment
About You
You are genuinely passionate about our purpose
You bring precision and excellence to all that you do
You believe in our rooted-in-science approach to problem-solving
You are a generous collaborator who can work in teams with a broad spectrum of backgrounds
You take pride in enabling the best work of others on the team
You can 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!
Locations
Genmab maximizes the efficiency of an agile working environment when possible for the betterment of employee work-life balance. Our offices are crafted as open community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether youre in one of our office spaces or working remotely we thrive on connecting with each other to innovate.
About Genmab
Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years its hard-working innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational quantitative and data sciences resulting in a proprietary pipeline including bispecific T-cell engagers antibody-drug conjugates next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030 Genmabs vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO) antibody medicines.
Established in 1999 Genmab is headquartered in Copenhagen Denmark with international presence across North America Europe and Asia Pacific. For more information please visit and follow us on LinkedIn and X.
Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice ().
Required Experience:
Contract
Employment Type
Contract
