Job details
Job type full-time
Full job description
Job details
Level
Experienced
Job location
Rockville, md - rockville, md
Remote type
Fully remote
Position type
Full time
Education level
Phd
Job category
Biotech job details
About us: champions oncology is a technology-enabled research organization that leverages an end-to-end range of research and development solutions to improve the productivity of oncology drug developmentUsing computational and experimental testing platforms, champions oncology improves decision making for effective therapeutic developmentOur team is passionate and self-motivated working together to accelerate the challenges of oncology drug development and ultimately improve patients’ lives around the world.
Title and classification: study director translational oncology solutions (tos) / exempt
Reporting location: remote, anywhere in the us
Primary objectives: the study director serves as the primary point of contact for champions vast portfolio of client sponsors regarding scientific design, pdx tumor model selection, and project executionThe study director is client facing and requires strong customer focus and an understanding of the needs and timelines of the clientThe study director provides expertise to clients on the uses of the tumorgraft/pdx mouse platform for preclinical drug testingEssential job duties include preliminary client study design in collaboration with the business development team, interaction with the lab and facilities operations teams to coordinate study execution, and preparing study protocols/updates/analyses/reportsCollaborates with the business development group to enhance client relationships and facilitate continued business for champions oncologyThe study director will be proactive with regards to client needs for ongoing and future studies, provide excellent customer service and mitigate miscommunications that occur in the preparation, execution and delivery of tos projectsDuties and responsibilities:
Participates as the scientific technical lead in client meetings related to potential and current pre-clinical pdx opportunities.
Manages studies with highly technical components and expanded endpoints such as immunograft and hematological studies involving ex-vivo analyses including but not limited to 2d/3d cell assays, luminex, elisa and flow cytometry.
Defines client scientific requirements and develops study design and protocols according to iacuc guidelines and operational ability.
Recommends tumor model selection based on needs and availability; suggests replacements when necessary.
Reviews formulation documents and ensures all necessary test agents and standards of care are in stock prior to study initiation.
Organizes kickoff and protocol review meetings with clients and internal staff.
Monitors ongoing study data to ensure tasks are being completed and any adverse events are identified and communicated to the sponsor in a timely manner.
Issues directives to the lab based on data and protocol endpoints.
Performs data and statistical analysis of study data at completion of tos sponsor studies.
Provide weekly updates, data analysis, and final reports to clients.
Recognizes revenue for models/studies for finance through salesforce.
Interfaces with business development, operations, and other champions personnel to successfully coordinate projects from start to finish
Identifies and provides resolution to problems involving ongoing tos studies.
Participates in discussions around and provides feedback for process improvement to improve quality.
Represents champions in the field at client meetings and scientific conferences.
Identifies potential new opportunities and facilitates ongoing discussions regarding new opportunities with existing clients.
Deliver customer value in a timely manner, and ensure protocols are accurate
Works independently and performs other related duties as assigned.
Knowledge, skills and abilities
Depth of scientific knowledge around preclinical research platforms.
Scientific expertise in molecular biology techniques including but not limited to those associated with cell-based assays, elisa, pcr, and ihc.
Experience with analyzing flow cytometry data a plus.
Knowledge of project management and oncology researchKnowledge of in vivo oncology models (xenograft/pdx) requiredUnderstanding of preclinical drug development a plus.
Customer service skills, timely decision making, good interpersonal skills and an ability to be persistent while maintaining tact.
Must have the ability to balance several priorities simultaneously with high attention to detail.
Ability for frequent adaptation, self-organization, accountability.
Effective oral and written communication skills are required.
Knowledge of microsoft word and excel as well as statistical software such as graphpad prism.
Education and experience
Ph.dDegree in chemical/biological science preferred.
3 to 5 years of experience in pre-clinical research or a similar position.
This job description may be changed to include new responsibilities and tasks or change existing ones as management deems necessary.
Champions oncology is an equal opportunity/ affirmative action employerWe celebrate diversity and are committed to creating an inclusive environment for all employees.
