POSITION SUMMARY:
Coordinates and conducts research protocols in a manner that ensures quality, consistency, timeliness, accuracy and patient safety.
PRIMARY JOB FUNCTIONS:
· Establishes and maintains frequent face-to-face, written and telephone contact with various persons involved in the study, including but not limited to the subjects, relatives/friends of the subjects, doctors, pharmaceutical sponsors, and pharmacists.
· Function in the role of Lead or co-lead on studies as assigned
· Identifies, evaluates and recruits qualified potential subjects for the clinical research study assigned
· Becomes thoroughly familiar with the regulatory documents, protocol, case report form, informed consent, source documentation, subject diary (when applicable), and study medication(s) for the assigned research study
· Coordinates and conducts pre-study, initiation, monitoring and close-out visits with the pharmaceutical representative, including completion of minutes and follow-up reports
· Performs appropriate research protocol procedures which may include, but are not limited to: vital signs, pregnancy tests, blood collection and processing, accountability of specimens and notification of courier for specimen pick-ups, ECGs, alcohol breath tests and pain assessments
· Provides Project managers with summary data related to all study activities
· Is responsible for high level administrative study oversight
· May aid in the development of Clinical Assistant and Clinical Coordinator l staff
· All other projects as assigned
EDUCATION/SKILL/EXPERIENCE REQUIREMENTS:
· Bachelors degree in Health Science or equivalent
· CPR certification
· CRC certification
· Phlebotomy certification (national) preferred
· Maintain current status of nursing license or paramedic certification (if applicable)
· Current LVN license or paramedic with 1 year minimum direct clinical research experience OR
· Bachelors degree in Health Science and a minimum of two years direct clinical research experience OR
· Excellent communication skills (interpersonal, written, verbal)
· Strong attention to detail
· Excellent time management and organizational skills
· Management and supervisory skills helpful
· Intermediate computer skills
· Minimum of two years as a Clinical Research Coordinator l
Join Aerotek Scientific LLCSM, one of the fastest growing providers of scientific and clinical research services in the nation. Due to our growth, we're constantly on the lookout for qualified professionals to place in contract, contract-to-hire, and permanent placement positions across the scientific and clinical research communities. At Aerotek Scientific, we know it's more than just your day-to-day responsibilities that can make or break a job. It's the support you get. That's the reason Aerotek Scientific offers a variety of benefits including medical, dental, optical, 401k, and many more. Don't put your career in the hands of just anyone, put it in the hands of a specialist. Join the Aerotek Scientific team! Allegis Group and its subsidiaries are equal opportunity employers.
Job Details |
Job Location |
Candidate Application |
| Employer: Aerotek Scientific | Address: 2525 W. Bellfort | Contact: Jerrell C. Branch |
| Job Type: Full-time | City: Houston | |
| Experience:Any | State: Texas | E-mail: jbranch@aerotek.com |
| Education: Bachelors Degree | Zip Code:77036 | Online: Website Link |
Rate: Based on experience.
If you wish, you may also Submit Your Resume to the Insourced co-branded Resume Submission service, which will make your resume available to all employers in the CareerBuilder.com job search system.
Insourced lists job information exactly as provided by employers.
Please click on the Job Source link to confirm the status of a position and to clarify any discrepancies or errors in a job post.
View all: Aerotek Scientific Jobs