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- Working independently and proactively to coordinate all necessary activities required to set up and monitor a study, completing accurate study status reports and maintaining study documentation
- Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
- Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
- Managing sponsor generated queries efficiently and responsible for study cost effectiveness
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- Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
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- Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner
- Ability to produce accurate work to tight deadlines within a pressurized environment
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Who we are
Salary
Location
Mexico
Department
Clinical Operations Roles
Location
Mexico
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
Reference
2024-110036
Expiry date
01/01/0001
Read more
Shortlist Save this role
Salary
Location
Mexico
Department
Clinical Operations Roles
Location
Mexico
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
Reference
2024-109897
Expiry date
01/01/0001
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Salary
Location
Mexico, Mexico City
Department
Full Service - Commercial Solutions
Location
Mexico City
Sofia
Remote Working
Office Based
Job Categories
Proposals
Job Type
Permanent
Description
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Salary
Location
Mexico City
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
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Remote Working
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Study Start Up
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