Full Job Description
About Us:
Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Job Summary:
Responsible for assisting with the implementation of clinical trials, serving as the authority for safety evaluations and study assessments on a daily basis or when the principal investigator is not present. Responsible for accurately documenting all information obtained throughout the clinical research process.
Essential Responsibilities and Duties:
Completes a company orientation program, prior to performing job responsibilities.
Responsible for the medical care of study patients, according to protocol requirements and/or site standing orders.
Completes source documents appropriately.
Recruits potential study subjects.
Screens, consents, and conducts study procedures, as designated on the Delegation of Authority Log.
Administers or coordinates the administration of investigational medication and follow subjects through the study period, per protocol.
Conduct required assessments throughout the clinical trial assessment period.
Responsible for maintaining and completing Case Report Forms in agreement with the source documentation and in accordance with study protocol.
Assures drug and clinical supply accountability for assigned trials.
Accompanies sponsors representatives during site visits and follows up, as needed.
Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings, and other meetings as assigned.
Observes, documents, reports, and follows up on adverse events and serious adverse
events.
Ensures proper collection, processing, and shipment (if applicable) of laboratory specimens, in coordination with Research Assistants/Study Coordinators, if applicable.
Follows up appropriately on all laboratory results.
Maintains infection control safety standards when performing job responsibilities.
Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Education/Experience/Skills:
Must be able to effectively communicate verbally and in writing.
Must be a physician, nurse practitioner or physician’s assistant with a current license in the state in which the employee will be working.
Must be capable of performing all clinical tasks relevant to licensure and/or training.
Must be able to clearly communicate verbally with patients.
Must have good interpersonal skills, demonstrated through interactions with patients, staff, Sponsor representatives, etc.
Must be self-motivated and able to perform tasks independently.
Must reflect the professional image of the company, upholding the company vision in
actions and demeanor.
Working Conditions
1. Indoor, Clinic environment.
2. Essential physical requirements include sitting, typing, standing, walking.
3. Lightly active position, occasional lifting of up to 20 pounds.
4. Reporting to work, as scheduled, is essential.
CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, nationalorigin, veteran, or status.
Job Type: Full-time
Pay: $120,000.00 – $135,000.00 per year
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Medical Specialty:
- Medical-Surgical
License/Certification:
- APRN (Preferred)
- PA-C (Preferred)
Ability to Commute:
- Salt Lake City, UT 84107 (Required)
Ability to Relocate:
- Salt Lake City, UT 84107: Relocate before starting work (Required)
Work Location: In person
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