Clinical Research Coordinator
AbbottAbout the role
JOB DESCRIPTION:
The Opportunity:
Our location in Alameda, California has an opportunity for an experienced professional in the Medical Affairs Sub-Function, who possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.
What you will do:
•Contributes to implementation of clinical protocols and facilitates completion of final reports.
•Recruits clinical investigators and negotiates study design and costs.
•Responsible for directing human clinical trials, phases III & IV for company products under development.
•Participates in adverse event reporting and safety responsibilities monitoring.
•Coordinates and provides reporting information for reports submitted to the regulatory agencies.
•Monitors adherence to protocols and determines study completion.
•Coordinates and oversees investigator initiations and group studies.
•May participate in adverse event reporting and safety responsibilities monitoring.
•May act as consultant/liaison with other corporations when working under licensing agreements.
Requirements:
Must have an Associate's Degree in a relatable field of study
0-2 years of experience in a similar role.
The base pay for this position is
$68,700.00 – $105,300.00In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Medical & Scientific Affairs
DIVISION:
ADC Diabetes Care
LOCATION:
United States > Alameda : 1360-1380 South Loop Road
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 20 % of the Time
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
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