Senior Clinical Trial Study Coordinator at Jobot
Los Angeles, CA 90057
About the Job
Top Pay for Bilingual Experience!
This Jobot Job is hosted by: Sarah Murphy
Are you a fit? Easy Apply now by clicking the "Quick Apply" button and sending us your resume.
Salary: $105,000 - $125,000 per year
A bit about us:
We are dedicated to conducting Phase II-IV and post-marketing clinical research in wide variety of therapeutic areas. Our fields of research interests include cardiology, allergy/asthma, GYN, pediatrics, dermatology, devices, endocrinology, gastroenterology, nephrology, urology, neurology, osteoporosis, pulmonary and rheumatology.
Comprised of a team of experienced medical professionals, we take pride in our commitment to excellent patient care, quality research, and in meeting early enrollment goals with evaluable patients.
Why join us?
Competitive compensation package
Flexible paid time off
Medical, Dental and Vision benefits
Reimbursable expenses to support travel as needed
Flexible career path
Job Details
Requirements:
5+ years of experience as a Study Coordinator
Bilingual Spanish/English required
Previous phlebotomy/blood draw experience
Ability to travel to all 3 clinic locations if needed
Key Responsibilities:
Study Planning and Implementation:
Collaborate with the principal investigator to design protocols and develop study plans.
Coordinate and manage study activities, ensuring adherence to timelines and protocols.
Assist in obtaining necessary regulatory approvals and documentation.
Participant Recruitment and Screening:
Screen and recruit eligible participants according to study criteria.
Coordinate participant visits, conduct informed consent processes, and ensure compliance with study protocols.
Data Collection and Management:
Oversee data collection procedures, ensuring accuracy and completeness.
Maintain detailed records of participant information, adverse events, and protocol deviations.
Perform data entry and manage study databases or electronic data capture systems.
Study Coordination and Communication:
Act as a liaison between research staff, study sponsors, regulatory authorities, and participants.
Schedule and coordinate site visits, meetings, and conferences related to the study.
Provide regular updates to the research team regarding study progress and milestones.
Compliance and Quality Assurance:
Ensure compliance with Good Clinical Practice (GCP), regulatory guidelines, and institutional policies.
Perform quality checks and audits to maintain data integrity and protocol adherence.
Assist in preparing for and participating in study-related audits and inspections.
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
This Jobot Job is hosted by: Sarah Murphy
Are you a fit? Easy Apply now by clicking the "Quick Apply" button and sending us your resume.
Salary: $105,000 - $125,000 per year
A bit about us:
We are dedicated to conducting Phase II-IV and post-marketing clinical research in wide variety of therapeutic areas. Our fields of research interests include cardiology, allergy/asthma, GYN, pediatrics, dermatology, devices, endocrinology, gastroenterology, nephrology, urology, neurology, osteoporosis, pulmonary and rheumatology.
Comprised of a team of experienced medical professionals, we take pride in our commitment to excellent patient care, quality research, and in meeting early enrollment goals with evaluable patients.
Why join us?
Competitive compensation package
Flexible paid time off
Medical, Dental and Vision benefits
Reimbursable expenses to support travel as needed
Flexible career path
Job Details
Requirements:
5+ years of experience as a Study Coordinator
Bilingual Spanish/English required
Previous phlebotomy/blood draw experience
Ability to travel to all 3 clinic locations if needed
Key Responsibilities:
Study Planning and Implementation:
Collaborate with the principal investigator to design protocols and develop study plans.
Coordinate and manage study activities, ensuring adherence to timelines and protocols.
Assist in obtaining necessary regulatory approvals and documentation.
Participant Recruitment and Screening:
Screen and recruit eligible participants according to study criteria.
Coordinate participant visits, conduct informed consent processes, and ensure compliance with study protocols.
Data Collection and Management:
Oversee data collection procedures, ensuring accuracy and completeness.
Maintain detailed records of participant information, adverse events, and protocol deviations.
Perform data entry and manage study databases or electronic data capture systems.
Study Coordination and Communication:
Act as a liaison between research staff, study sponsors, regulatory authorities, and participants.
Schedule and coordinate site visits, meetings, and conferences related to the study.
Provide regular updates to the research team regarding study progress and milestones.
Compliance and Quality Assurance:
Ensure compliance with Good Clinical Practice (GCP), regulatory guidelines, and institutional policies.
Perform quality checks and audits to maintain data integrity and protocol adherence.
Assist in preparing for and participating in study-related audits and inspections.
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
Salary
105,000 - 125,000 /year