What's your preference?
Job Description
- Req#: JR141913
Employer Industry: Clinical Research Organization
Why consider this job opportunity:
- Competitive salary and benefits package designed for well-being and work-life balance
- Opportunity for career advancement and growth within a leading clinical research organization
- Comprehensive health insurance offerings tailored to suit you and your family's needs
- Global Employee Assistance Programme providing 24-hour access to a network of specialized professionals for well-being support
- Various annual leave entitlements and flexible optional benefits such as childcare vouchers and discounted gym memberships
- Inclusive and supportive work environment that values diversity and fosters innovation
What to Expect (Job Responsibilities):
- 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 resolve queries to maintain high-quality clinical data
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports
What is Required (Qualifications):
- Bachelor’s degree in a scientific or healthcare-related field highly preferred
- 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 travel at least 60% of the time (international and domestic) and possess a valid driver's license
How to Stand Out (Preferred Qualifications):
- Experience working in a fast-paced clinical research environment
- Familiarity with electronic data capture systems and clinical trial management software
- Demonstrated ability to work both independently and as part of a collaborative team
- Previous experience in ophthalmology-related clinical trials
#ClinicalResearch #HealthcareIntelligence #CareerOpportunity #DiversityAndInclusion #ClinicalTrials
"We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately. We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer."About the company
The best remote jobs for you
Notice
Talentify is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Talentify provides reasonable accommodations to qualified applicants with disabilities, including disabled veterans. Request assistance at accessibility@talentify.io or 407-000-0000.
Federal law requires every new hire to complete Form I-9 and present proof of identity and U.S. work eligibility.
An Automated Employment Decision Tool (AEDT) will score your job-related skills and responses. Bias-audit & data-use details: www.talentify.io/bias-audit-report. NYC applicants may request an alternative process or accommodation at aedt@talentify.io or 407-000-0000.