Senior Clinical Research Associate

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations

• Advanced degree in a relevant field such as life sciences, nursing, or medicine
• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
• Phase I Oncology Expertise: Strong background in early-phase oncology trials, including safety, PK/PD, and dose-escalation studies
• Indication-Specific Knowledge: Experience with breast, ovarian, prostate, and pancreatic cancer clinical trials
• Traditional Monitoring Model: Solid skills and proficiency in on-site monitoring, full source data verification, IP accountability and regulatory compliance
• Trip Report Writing: Proven ability to produce detailed, accurate, and timely monitoring visit reports. Extensive experience working with a CTMS platform (Siebel CTMS, Veeva Vault CTMS, Medidata CTMS, Oracle Clinical/Clinical One, or others)

Investigational Product Familiarity: Prior exposure to PARP inhibitors (a plus but not mandatory)

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others