Study Coordinator, PL

Champions Oncology Inc.; Rockville (MD); Remote; USD 50,000 - 65,000; Full time

Job summary

Champions Oncology, Inc. seeks a Study Coordinator for Translational Oncology Solutions in Rockville, MD with remote options. You will support the Project Leadership team, manage study timelines, enter data, and coordinate scheduling and study execution across internal groups and external collaborators.

The role requires a BS or MS in biology/chemistry, 1–3 years CRO/pre-clinical experience preferred, and strong communication. Word/Excel proficiency is essential; oncology experience is a plus.

Qualifications

• BS degree with appropriate experience or MS with focus in biology/chemistry; oncology a plus.
• 1–3 years CRO/pre-clinical experience preferred but not required.
• Strong communication, organization and ability to manage multiple priorities.
• Proficiency in Microsoft Word and Excel.

Responsibilities

• Support Project Leadership by coordinating scheduling and study execution.
• Enter study information into databases and monitor timelines.
• Plan and schedule studies with operations teams and update protocols as needed.
• Work with LIMS for study management and enrollment activities.
• Coordinate shipment of samples and liaise with collaborators and clients.

Skills

Project management

Oncology research

In vivo models

Communication

multitasking

Education

BS or MS in biology/chemistry

Tools

Microsoft Word

Excel

Job description

TITLE: Study Coordinator Translational Oncology Solutions (TOS)

REPORTING LOCATION:

Rockville, MD / Remote, US

REPORTS TO:

Manager of Project Leadership

SALARY RANGE:

$50,000 - $65,000 yearly

PRIMARY OBJECTIVES

The Study Coordinator (SC) serves as the primary supporting role for the Project Leadership team who manages Champions vast portfolio of client sponsors regarding scientific design, PDX tumor model selection, and project execution. The SC will work closely with the Project Leaders/Study Directors and requires strong communication skills, attention to detail and the need to be highly organized. The SC will also interact and liaise with various internal operations groups at Champions to coordinate the scheduling/planning and execution of studies.

DUTIES AND RESPONSIBILITIES

To support the Project Leadership team, duties and responsibilities will include:

• Initial entry of study information into database(s) for project management purposes.
• Assist in generating estimated study timelines.
• Assist in planning/scheduling of studies in coordination with project leadership and operations teams.
• Update study information as needed to capture protocol amendments.
• Manage and update project timelines and milestones within database(s).
• Work with operations for procurement of materials required for study execution.
• Create initial study protocol drafts and amendments as appropriate.
• Manage aspects of ongoing studies in the laboratory information management system in partnership with the Project Leader.
• Perform and/or review enrollment of in vivo studies.
• Assist in scheduling end of study activities/analyses with various operational groups.
• Work with logistics to arrange shipment of samples to collaborators and clients/laboratories for studies.
• Identifies and provides resolution to problems involving ongoing studies, as appropriate.
• Participates and provides feedback in team meetings
• Works independently and performs other related duties as assigned.

KNOWLEDGE, SKILLS AND ABILITIES

• Knowledge of project management and oncology research. Knowledge of in vivo oncology models (Xenograft/PDX) preferred.
• Ability to work in multiple databases to assist in project management.
• Collaborative, can-do attitude. 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.
• Proficiency in using Microsoft Word and Excel.

EDUCATION AND EXPERIENCE

• B.S. degree with appropriate experience or M.S. degree with a focus on a biology or chemistry related field, oncology a plus.
• 1 to 3 years of experience in the field of contract research, pre-clinical research or a similar position is preferred but not required.

PHYSICAL DEMANDS AND WORK ENVIRONMENT:

• Must be able to sit for long periods of time using a computer in a typical office environment in a multi-level facility or home office.

This description reflects management's assignment of essential functions, it does not proscribe or restrict the tasks that may be assigned. We celebrate diversity and are committed to creating an inclusive environment for all employees.