Clinical Research Coordinator Job at Moffitt Cancer Center, Tampa, FL

MjdCMUVwVXYwVldFM3VBRUNYRzA4TG92aUE9PQ==
  • Moffitt Cancer Center
  • Tampa, FL

Job Description

Are you looking for an opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial. You will be the member of the Team that ensures the trial is moving forward safely, smoothly, and according to plan. 

Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities. The Clinical Research Coordinator role is a terrific opportunity for those who have already worked in other areas of healthcare as well as those who are looking for a new and exciting way to contribute through their career.

This position offers a Monday through Friday schedule and hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period. Moffitt offers paid training and orientation through its CTO (Clinical Trails Office) Academy. Position tiers may vary according to experience. Relocation assistance may be provided. 

These positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers.

Successful candidates will possess: 

  • Effective communication, good decision making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and time management skills 
  • Excellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiences 
  • Prior experience in clinical trials is preferred 
  • Familiarity with regulatory requirements in clinical research or ability to successfully learn this
  • Experience interacting with patients and coordinating care with medical staff 
  • Gain a solid learning and understanding of regulatory guidelines and following a clinical trial protocol 

Education and experience requirements per tier: 

Clinical Trials Screening Coordinator: 

  • Bachelor’s degree required, 2 years of experience in clinical trials (patient facing coordination, data management, regulatory or other research coordination). Knowledge of the clinical research process, procedures, and protocols.

Associate Clinical Research Coordinator: 

  • Associates degree required, in lieu of Associates degree 2 years of relevant experience with a high school diploma or GED. Experience with data entry, good oral and written communication skills and organizational skills.

Clinical Research Coordinator I: 

  • Bachelor's Degree with one (1) year of relevant clinical, health related, scientific, business or research experience. In lieu of a bachelor's degree, Associates degree with an additional year of relevant experience for a total of two (2) years of experience. 

Clinical Research Coordinator II: 

  • Bachelor's degree with 2 years clinical trials coordination experience. In lieu of a bachelor's degree, an associate degree with 4 years of clinical trials coordination experience may be considered.

  • CCRP/CCRC or equivalent preferred. 

Clinical Research Coordinator III: 

  • Bachelor’s degree with 4 years of experience in clinical trials coordination. In lieu of a bachelor’s degree, associate degree with 6 years clinical trials coordination experience may be considered. 

  • CCRP/CCRC certification required

Clinical Research Coordinator Sr.: 

  • Bachelor's degree with 6 years of experience in clinical trial coordination. In lieu of a Bachelors' degree, associate degree with an additional 2 years of clinical trials coordination experience for a total of 8 years of experience may be considered. 
  • CCRP/CCRC certification required 

Job Tags

Full time, Remote job, Relocation package, Monday to Friday,

Similar Jobs

Wayfair

Training Coordinator Job at Wayfair

 ...We are the front-line leaders in the Wayfair Global Supply Chain Workforce Support Network, providing direct training & development support to our Supply Chain teams! We bring network-wide resources along with realistic and challenging training initiatives to optimize... 

Quick Hire Staffing

Robotic Weld Tech - $70K salary Job at Quick Hire Staffing

 ...Robotic Weld Tech is responsible for the operation and maintenance of robotic welding equipment and related equipment. This position...  ...quality regulations. Requirements Service, maintain, repair, install and test new or existing equipment and verify conformance to... 

BearingPoint Consulting, Inc. USA

Data Science Manager Job at BearingPoint Consulting, Inc. USA

 ...A candidate for this role should have a comprehensive knowledge of data science and advanced analytics, as well as a high-level vision to shape data science offerings, build data capabilities, and grow data business. They should be able to create and sell datapropositions... 

Creattix Talk

Data Entry Clerk Job at Creattix Talk

 ...Job Title: Data Entry Clerk Location: Miami FL Company: Creattix Talk Job Description: We are seeking a detailoriented...  ...Requirements: High school diploma or equivalent. Excellent typing skills and proficiency in MS Office (Word Excel Outlook... 

Laserfiche

Junior LMS Administrator Job at Laserfiche

DescriptionThe Junior LMS Administrator maintains and supports the learning management system (LMS) to meet regulatory compliance needs and ensure data accuracy and integrity. The LMS serves both our internal Laserfiche employees and our Laserfiche users, so this...