Clinical Research Associate II
Behavioral Health Market Context
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Benefits
In addition to your competitive salary, ICON offers a range of additional benefits focused on well‑being and work‑life balance for you and your familyVarious annual leave entitlementsHealth insurance offerings to suit you and your family’s needsCompetitive retirement planning offeringsGlobal Employee Assistance Programme, Life Works, offering 24‑hour access to a global network of professionals supporting well‑beingLife assuranceFlexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others4 more items(s)
Qualifications
- •You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills
- •Bachelor's degree in a scientific or healthcare‑related field
- •Minimum of 2 years of experience as a Clinical Research Associate
- •In‑depth knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines
- •Strong organizational and communication skills, with attention to detail
- •Ability to work independently and collaboratively in a fast‑paced environment
- •Willingness to travel as required (approximately 60%)
- •4 more items(s)
Responsibilities
- •You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively
- •Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials
- •Ensure protocol compliance, data integrity, and patient safety throughout the trial process
- •Collaborate with investigators and site staff to facilitate smooth study conduct
- •Perform data review and resolution of queries to maintain high‑quality clinical data
- •Contribute to the preparation and review of study documentation, including protocols and clinical study reports
- •3 more items(s)
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