Clinical Research jobs
- ICON PlcSingapore
- Health insurance
- Vision insurance
- Dental insurance
- ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
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- National University of SingaporeQueenstown
- Familiarity with clinical research protocols, standard operating procedures, and good clinical practice.
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- National University of SingaporeQueenstown
- Familiarity with clinical research protocols, standard operating procedures, and good clinical practice.
- Introduction and improvement of biological, clinical,…
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View similar jobs with this employerNational Healthcare GroupSingapore- The role encompasses both research coordination and pathology/laboratory-based research support, including digital slide preparation and image management.
- IQVIASingapore
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View similar jobs with this employerNational University of SingaporeQueenstown- The successful candidate will contribute to a multidisciplinary translational research programme integrating patient-derived clinical specimens, advanced…
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- DEEP INTELLIGENT PHARMA (SG) PRIVATE LIMITEDSingapore
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Job Post Details
Clinical Research Associate - job post
Job details
Job type
- Full-time
Location
Benefits
Pulled from the full job description
- Health insurance
- Vision insurance
- Dental insurance
Full job description
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.
What you will be doing
- Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
- Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
- Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
- Ensure patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements.
Your profile
- At least 2 years of monitoring experience as a CRA.
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
- Excellent written and verbal communication in English
- Good social skills enabling you to deal with queries in a timely manner
- Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.