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Study Coordinator, Study Management

Champions Oncology

Rockville, MD, US
  • Job Type: Full-Time
  • Function: Operations
  • Industry: Life Sciences
  • Post Date: 09/23/2022
  • Website: championsoncology.com
  • Company Address: One University Plaza, Suite 307, Hackensack, NJ, 07601

About Champions Oncology

Champions Oncology, Inc. provides an end-to-end range of research and development solutions and services that improve the productivity of oncology drug development. Using both in vitro to in vivo testing platforms companies can leverage the expertise at Champions Oncology to help guide decision making for clinical development scenarios.

Job Description

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 development. Using computational and experimental testing platforms, Champions Oncology improves decision making for effective therapeutic development. Our team is passionate and self-motivated working together to accelerate the challenges of oncology drug development and ultimately improve patients’ lives around the world.

 

REPORTING LOCATION

Rockville, MD                                 

 

PRIMARY OBJECTIVES

Support in vivo oncology studies in mice as member of the Study Management team. Duties and responsibilities are:

  • Assist with all functions related to study phase management

  • Ensure timely preparation of stock, pre-study, and study phases

  • Coordinate with Operations, supporting labs, and Project Leadership to ensure accurate study set-up

  • Prepare, coordinate, and maintain critical timelines for execution of study.  Update and maintain dates in SF

  • Provide feedback/suggestions on Stock and Pre-study cohorts

  • Assist with improving productivity and increase efficiency, provide metrics as necessary 

  • Assist in the monitoring and measuring of model failures and revenue delays through a variety of knowledge-based tools (such as study overage, discontinuation of models, and study criteria)

  • Monitor, make recommendations, and develop solutions (to mitigate the risks to study delays) for any roadblocks that would inhibit a study date being met

  • Communicate changes for affected departments

  • Maintain and update databases and or other tools as required

  • Assist in training new staff

  • Provide project management and liaise with different in vivo departments including Project Leadership

  • Assist in creating and reviewing Standard Operating Procedures (SOPs)

  • Daily data review

  • Work weekend and holidays as needed

  • Perform all other related duties as assigned

KNOWLEDGE, SKILLS, AND ABILITIES

  • BS degree in biology, pharmacology, or related field, or minimum of 2 years of related experience
  • Experience in contract research animal facility or industry setting is preferred
  • Experience with preclinical in vivo pharmacology or oncology studies
  • Data analysis skills
  • Ability to work effectively and productively in a team-oriented environment while maintaining a strong sense of accountability, integrity and confidentiality.
  • Creative problem-solving skills and the ability to exercise sound and accurate judgment in making timely decisions.
  • Superior planning, organizational, computer, written, and verbal communication skills
  • Ability to handle multiple projects, prioritize work, and meet deadlines
  • Computer proficiency in MS Word, Excel, Outlook, and Sharepoint
  • Proficiency in LIMS and procedures used to accomplish data reduction
  • Ability to assist with other duties in a dynamic environment

 

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 Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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