Study Coordinator, PL

Oncology Voice Network LLC

Rockville (MD)

Hybride

USD 50 000 - 65 000

Plein temps

14 jours+

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Résumé du poste

Oncology Voice Network LLC is seeking a Study Coordinator for Translational Oncology Solutions in Rockville, MD. You will support the Project Leadership team, manage study data, timelines, and coordination across operations, procurement, and labs.

The role requires strong communication, organization, and attention to detail, with 1–3 years in contract research or pre-clinical settings preferred. Remote work option available.

Qualifications

  • Knowledge of project management and oncology research.
  • Experience with in vivo oncology models (Xenograft/PDX) preferred.
  • Proficiency with Microsoft Word and Excel.

Responsabilités

  • Enter study information into databases for project management.
  • Assist in estimating study timelines.
  • Plan and schedule studies with project leadership and operations.
  • Update study information for protocol amendments.
  • Manage project timelines and milestones in databases.
  • Coordinate procurement of materials for study execution.
  • Create initial study protocol drafts and amendments.
  • Manage LIMS aspects with the Project Leader.
  • Assist in enrolling in vivo studies.
  • Schedule end-of-study activities and analyses.
  • Coordinate shipment of samples to collaborators and labs.
  • Identify and resolve problems in ongoing studies.
  • Participate in team meetings.
  • Work independently and perform other duties as assigned.

Connaissances

Project management knowledge
Oncology research
In vivo models
Interpersonal skills

Formation

Bachelor's degree in biology/chemistry or related field
MS in biology/chemistry (preferred)

Outils

Microsoft Word
Excel

Description du poste

## Job DescriptionTITLE: 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. Qualifications 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.
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