Celerion

Medical Research Assistant

Celerion  •  Tempe, AZ (Onsite)  •  3 hours ago
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Job Description

Celerion is committed to swift, exceptional clinical research through translational medicine.  Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.  
Medical Research Assistants will monitor activities of study participants, handle human biological samples and record data. Responsibilities also include taking vital signs, performing ECGs, phlebotomy, height/weight, and monitoring meals. We are seeking both part-time and full-time availability. Excellent training is provided.  Previous medical experience is preferred, but not required.

Requirements

  • High school diploma or GED
  • Post high school education in life sciences or medical training preferred
  • CPR certification preferred
  • Experience in accurate documentation of data preferred
  • Must be 18 years of age
  • Spanish-English bilingual fluency is preferred, but not required.
  • The Part-time role works ~24+ hours per week.
  • Weekend availability is required. 

Please Note

  • We currently part-time positions available. We have openings for AM and ON schedules (6:00am-2:30pm, and 10:00pm-6:30am).
  • Paid training occurs in the initial 6 weeks, at the same shift time. Scheduling during training is full-time.
  • Once training concludes, the regular work schedule is 24+ hours per week, based on your provided availability.
  • Seeking Part-time availability
Celerion Values:       Integrity   Trust   Teamwork   Respect
Are you ready to join our team?
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
Celerion

About Celerion

Celerion, a leader in early clinical research, delivers Applied Translational Medicine. Celerion applies our expertise and experience to translating information gained in research discoveries, to knowledge of drug action and effect in humans to support early drug development decisions and the clinical pharmacology labeling of new medicines.

With over 50 years of experience and 600 global clinic beds (including 24 in-hospital), Celerion conducts and analyzes First-in-Human, clinical proof-of-concept, cardiovascular safety (TQT, robust QT), ADME and NDA-enabling clinical pharmacology studies. Celerion provides expertise on modeling and simulation, study design, medical writing (protocols and reports), clinical data sciences, biostatistics, and PK/PD analysis as well as small and large molecule bioanalytical assays through clinical drug development. Regulatory, drug development and program management complement Celerion’s service offerings.

Our operations are strategically located in:

Lincoln, Nebraska (Corporate Headquarters)

Philadelphia, Pennsylvania

Phoenix, Arizona

Belfast, Northern Ireland,UK

Zurich, Switzerland

Vienna, Austria

Richmond, Virginia

Montreal, Quebec, Canada

For more information, visit: www.celerion.com

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Lincoln, NE
Year Founded
2010
Website
celerion.com
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