You are viewing a preview of this job. Log in or register to view more details about this job.

Clinical Research Coordinator -

Clinical Research Coordinator - LSR

Job ID
2019-1226
Category Clinical Research Location : Location
 US-NM-Albuquerque Type Full-time Company/Division Lovelace Scientific Resources (LSR)

Overview

Lovelace Scientific Resources (LSR), a subsidiary of the Lovelace Respiratory Research Institute (LRRI), is seeking a full time Clinical Research Coordinator to oversee the regulatory aspect of clinical trials.
 
The Clinical Research Coordinator will work under the supervision of the President and will support regulatory affairs activities and provide administrative support to the Site.
 
Duties include, but not limited to, collecting and reviewing subject’s clinical data; performing clinical tasks such as ECG’s, vital signs, participant interviews and assessment, phlebotomy, and other specialized testing; recruiting for studies , prescreening and recruiting potential subject participants for clinical research studies; word processing, telephone and reception, maintaining required regulatory documents, proficient in computer skills such as data entry, and performing all other related duties and tasks as required or assigned.
 
Regulatory duties include but not limited to, initial internal Review Board (IRB) submissions, maintenance of the Investigator Site File (ISF), track Good Clinical Practices, Sponsor and Site training based on the International Conference of Harmonisation (ICH) guidelines.  
 
 

Qualifications

Requires one year education or training in an allied health discipline such as Nursing, Biology, or a Paramedic and a minimum two years prior experience in a clinical research setting or equivalent combination of education, training and/or experience from which comparable knowledge, skills and abilities have been attained. CPR Basic Life Support certification required.
 
Must understand the Code of Federal Regulations as it relates to clinical research.
 
Must have demonstrated experience interfacing with other health professionals in the research setting, fundamental understanding of medical terminology, research regulations, and healthcare practices, and previous experience working in a fast-paced clinical research setting id highly desirable. Individual must be able to handle high volume and level of administrative tasks. 
 
The Clinical Research Coordinator must have outstanding customer service skills and the ability to maintain complete confidentiality of Site research documents, patient records if applicable, and research and regulatory data. Must have strong verbal and written communication skills, professional-level proficiency computer skills and advanced experience with Microsoft Office and working in spread sheets and databases with the ability to learn department-specific computer systems as needed.
 
Candidates who have experience as a Clinical Research Coordinator and have an interest in Regulatory Affairs within clinical research are encouraged to apply. 

Preferred/Additional Qualifications

Certification in clinical research is highly desirable. Medical certifications Licensure such as a Registered Nurse, or Licensed Vocational Nurse with clinical research experience is preferred.

Salary

Salary is commensurate with experience.
 

Equal Opportunity Employer

The Lovelace Respiratory Research Institute Family of Companies is an Equal Opportunity employer–M/F/Veteran/Disability. We are committed to the hiring, advancement and fair treatment of all individuals, and all qualified applicants will receive consideration for employment without regarding to race, color, religion, sex, national origin, sexual orientation, gender identity, age, disability, protected veteran status, or any other protected status as designated by federal, state or local law. All applicants and employees are further protected from discrimination based on inquiring about, disclosing or discussing the compensation of other applicants or employees. For additional information about your rights as an applicant, click here.

For assistance with our application process, including reasonable accommodations for individuals with disabilities to participate in the application process, please send an email to recruiting@lrri.org or call 505-348-9400.