Clinical Research Coordinator

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! In this role, you will assist I the management of the clinical aspects of the clinical trials conducted at QPS MRA. As a resource for the protocols, you will act as liaison between the investigators, primary care providers, vendors, the institutional review board (IRB), and the sponsor.

QPS' Story:

Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of services, including Early Phase Clinical and Phase II - IV Clinical Research services. The QPS location in Miami, Florida is a multi-specialty research center employing clinical research professionals, including board-certified physicians, in a 32,000 square foot space. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.

Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.

If this sounds like your ideal work environment, then we would love to speak with you, so apply today!

Please visit our website (www.qps.com) for more information and to see all current openings.

The Job

• Screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are in study.

• Work with ancillary research staff performing specific study roles.

• Maintenance of accurate and complete documentation, including not but limited to regulatory documents, signed informed consent forms, relevant IRB approvals, source documentation, drug dispensing logs, subject logs, and study-related communications.

• Organizational management of all aspects of the trial, including but not limited to timeliness in completing case report forms , data entry, reporting AEs and SAEs, managing caseload and managing study files.

• Communication of all protocol-related issues/problems to the Principal Investigator, Sub-Investigator, and/or appropriate management staff, including but not limited to questions regarding the conduct of the clinical trial, concerns regarding possible AEs, SAEs or subject compliance.

Requirements

• Bachelor's degree in related discipline, ideal

• A background as a registered nurse or LPN with a current license to practice, medical assistant, or

• Must possess effective communication skills (written and verbal).

• Bilingual English and Spanish is preferred.

• Minimum 1-3 years Clinical Research Experience.

Why You Should Apply

• Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.

• Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.

• Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance

QPS is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.