Oncology - Clinical Research Scientist
Company Name:
ImClone
Company Overview:
ImClone Systems LLC is a leader in therapeutic monoclonal antibodies and committed to changing the world of cancer care by developing a portfolio of targeted biologic treatments designed to address the medical needs of patients with a variety of tumor types. Founded in 1984, ImClone has a rich culture of discovery and deep expertise in oncology. Following its acquisition by Eli Lilly and Company in 2008, ImClone is accelerating its antibody pipeline development by leveraging Lilly's global capabilities. ImClone's pipeline has several molecules in mid- to late-stage clinical development targeting a variety of cancers.
Responsibilities:
Lead cross-functional technical assessment and prioritization of novel combination opportunities
Drive prioritization process for preclinical and clinical study recommendations
Partner with Lilly product / project teams to access internal portfolio assets for preclinical / clinical investigations
Partner with business development to access prioritized external assets
Represent ramucirumab Medical team in negotiations with third parties
Lead establishment of clinical development strategy and detailed study plan with internal / external collaborators
Lead establishment and delivery of program communication and disclosure plan
Collaborate with Project Management to develop defined timelines, scope, and budgets for all efforts
Collaborate with Project Management to achieve Product Team, Business Unit and Corporate approvals as necessary.
Other CRS
Responsibilities:
Clinical Planning
Trial Execution and Support
Scientific Data Dissemination and Exchange
Regulatory Support
Business/Customer Support
Scientific/Technical Expertise and Continued Development
Basic
Qualifications:
Advanced health/science/medically-related graduate degree or doctorate, including DVM, PharmD, PhD or Masters in Nursing.
Examples of relevant science degrees include Microbiology, Physiology, and Pharmacology. Qualified applicants will have one of the following:
o 3-5 Years of Clinical Experience
o 3-5 years of Pharmaceutical Experience (2 of which is in clinical development)
OR
o Have a BS or Masters Degree in a health/science/medically related field and 7-10 years of pharmaceutical experience that is directly related to at least one of the following:
o Clinical trial experience
o Experience in areas relevant to drug discovery
o Drug or clinical development experience (for example, pharmacology, epidemiology, toxicology, regulatory affairs)
Additional Skills/Preferences:
Position is based in New Jersey
Demonstrated ability to design early / mid-phase clinical studies
Demonstrated ability to lead cross function and external collaborations
Strong organizational skills
Ability to manage in a matrix organization
Strong communication skills
Ability to travel domestically and internationally to the degree required to support the business.
Must be fluent in English, verbal and written communication
Additional Information:
Eli Lilly and Company, Lilly USA LLC, affiliates and our wholly owned subsidiaries including ImClone Systems (collectively, Lilly) are EEO/Affirmative Action Employers, and do not discriminate on the basis of race, gender, protected veteran status, disability or any other legally protected status.
Apply online at:
https://xjobs.brassring.com/tgwebhost/jobdetails.aspx?PartnerId=25428&SiteId=5645&Areq=11715BR&Codes=IMBEstimated Salary: $20 to $28 per hour based on qualifications.
ImClone
Company Overview:
ImClone Systems LLC is a leader in therapeutic monoclonal antibodies and committed to changing the world of cancer care by developing a portfolio of targeted biologic treatments designed to address the medical needs of patients with a variety of tumor types. Founded in 1984, ImClone has a rich culture of discovery and deep expertise in oncology. Following its acquisition by Eli Lilly and Company in 2008, ImClone is accelerating its antibody pipeline development by leveraging Lilly's global capabilities. ImClone's pipeline has several molecules in mid- to late-stage clinical development targeting a variety of cancers.
Responsibilities:
Lead cross-functional technical assessment and prioritization of novel combination opportunities
Drive prioritization process for preclinical and clinical study recommendations
Partner with Lilly product / project teams to access internal portfolio assets for preclinical / clinical investigations
Partner with business development to access prioritized external assets
Represent ramucirumab Medical team in negotiations with third parties
Lead establishment of clinical development strategy and detailed study plan with internal / external collaborators
Lead establishment and delivery of program communication and disclosure plan
Collaborate with Project Management to develop defined timelines, scope, and budgets for all efforts
Collaborate with Project Management to achieve Product Team, Business Unit and Corporate approvals as necessary.
Other CRS
Responsibilities:
Clinical Planning
Trial Execution and Support
Scientific Data Dissemination and Exchange
Regulatory Support
Business/Customer Support
Scientific/Technical Expertise and Continued Development
Basic
Qualifications:
Advanced health/science/medically-related graduate degree or doctorate, including DVM, PharmD, PhD or Masters in Nursing.
Examples of relevant science degrees include Microbiology, Physiology, and Pharmacology. Qualified applicants will have one of the following:
o 3-5 Years of Clinical Experience
o 3-5 years of Pharmaceutical Experience (2 of which is in clinical development)
OR
o Have a BS or Masters Degree in a health/science/medically related field and 7-10 years of pharmaceutical experience that is directly related to at least one of the following:
o Clinical trial experience
o Experience in areas relevant to drug discovery
o Drug or clinical development experience (for example, pharmacology, epidemiology, toxicology, regulatory affairs)
Additional Skills/Preferences:
Position is based in New Jersey
Demonstrated ability to design early / mid-phase clinical studies
Demonstrated ability to lead cross function and external collaborations
Strong organizational skills
Ability to manage in a matrix organization
Strong communication skills
Ability to travel domestically and internationally to the degree required to support the business.
Must be fluent in English, verbal and written communication
Additional Information:
Eli Lilly and Company, Lilly USA LLC, affiliates and our wholly owned subsidiaries including ImClone Systems (collectively, Lilly) are EEO/Affirmative Action Employers, and do not discriminate on the basis of race, gender, protected veteran status, disability or any other legally protected status.
Apply online at:
https://xjobs.brassring.com/tgwebhost/jobdetails.aspx?PartnerId=25428&SiteId=5645&Areq=11715BR&Codes=IMBEstimated Salary: $20 to $28 per hour based on qualifications.
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