Actalent Hiring for Clinical Research Coordinator at Washington, District Of Columbia Full Time

Re-locating opportunity

Description:

Clinical Research Design and Administration

Implementation of oncology clinical research requires planning and teamwork in order to assure patient safety and research quality. The Study Coordinator coordinates multiple complex trials through the protocol life cycles of activation, implementation and closure. These trials are complex, requiring full knowledge of both GCP and full knowledge of individual research protocols; consequence of error could be significant physical harm to research subjects.

Study Coordinators independently plan, organize, and evaluate implementation of multiple oncology clinical research projects with knowledge of, and in compliance with, sponsor requirements. For each trial, acquire full knowledge of research protocol and related documents, plan and document methodologies for research subject and data management based on this knowledge.

Study Coordinators train others in research methodology and direct the work of team members and staff from other services to complete research goals.

Training, Communication & Instruction

*Serve as content expert for multiple, complex trials; instructing other members of research team as well as staff from other services which interface in conducting oncology clinical research

*Establish communication systems and lead conversations to ensure complete execution of all aspects of trial conduct. Develop tools to gather required data and to facilitate compliant conduct of clinical research; educate team on procedures.

*Facilitate meetings between sponsors, investigators, and research team to assess feasibility and design of the protocol. Attend Investigators’ Meetings and teach others based on knowledge obtained. Lead start-up meetings and other on-site with the Protocol Office research team, Principal Investigator and auxiliary departments when their services are required; instruct team in coordinative aspects of the protocol and conduct training across services.

Education patients about participating in a research study to ensure patient safety and improve protocol compliance

Skills:

CCRC, Oncology, Clinical Research Coordinator, Clinical Research

Top Skills Details:

CCRC, Oncology, Clinical Research Coordinator

Additional Skills & Qualifications:

Instruction: This position requires the ability to train others in the performance of methodologies necessary to conduct clinical research and to document research methodologies. These skills are required to develop Subject and Data Management Plans, t

Experience Level:

Intermediate Level

About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.