CLINICAL RESEARCH COORDINATOR I

H. Lee Moffitt Cancer Center

Tampa, FL

Job posting number: #7137295 (Ref:hlj_44162)

Posted: March 31, 2023

Application Deadline: Open Until Filled

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. 

https://moffitt.org/clinical-trials-research/clinical-trials/clinical-trials-administration/ 

Clinical Trials 

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 

 

The Hem/Myeloma Data Management department in the Clinical Trials Office is looking for a Clinical Trials Coordinator I.  

Position Highlights:

  • Will serve as the centralized point of contact for communication regarding clinical trials in the start-up process.
  • Facilitates the execution of opening clinical trials to accrual within the designated program patient population.
  • Communicates protocol specific information to primary clinical trial coordinator and principle investigator during the start-up phase of the protocol.
  • Will work with general guidance from supervisor to implement clinical trials through pre-site selection, SRC review, IRB approval, collaboration with ancillary departments, creation of protocol orders and other source documentations and finally SIV and protocol activation.

Ideal Candidate:

  • Will have in-depth knowledge of good clinical practices as set forth by Federal regulations.
  • Previous coordinator experience, oncology background preferred.
  • Engaged, organized individual with strong critical thinking skills who has the ability to work efficiently under pressure.
  • Highly motivated, shows initiative, is proactive and able to work independently as well as in a team.

Responsibilities:

  • Coordinate clinical research protocols throughout the start-up phase of the trial
  • Work collaboratively with specific departments to help maintain appropriate documents.
  • Verify the accuracy and completion of documentation including but not limited to, subject eligibility checklist, source documentations, drug dispensing logs, subject screening logs, and study-related communication. 
  • Will interact directly with patients, study sponsors, managers and other department personnel.

Credentials and Qualifications:

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



Mission To create a Moffitt culture of diversity, equity, and inclusion as we strive to contribute to the prevention and cure of cancer. Vision To advance and accelerate a culture of access, equity, and inclusion. Diversity is a priority at Moffitt and is meant "to promote a culture of diversity and inclusion as we contribute to the prevention and cure of cancer." The Enterprise Equity Department focuses its efforts on eliminating those obstacles to an individual’s ability to exist within their personal comfort zone at the cancer center. Everyone is important to meeting this priority. Addressing and responding to diversity and inclusion fosters an environment where mutual respect for diverse cultures, communication styles, languages, customs, beliefs, values, traditions, experiences and other ways in which we identify ourselves, is the expectation.


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