Senior Oncology CRA I/II — Remote Trial Leadership

Parexel International; United Kingdom; Remote; GBP 42,000 - 64,000; Full time

Benefits offered by this job

Car or Car Allowance

Medical & Dental Insurance

Life Assurance

Pension

Critical Illness Insurance & HealthSc

Health Screenings

Job summary

Parexel International is seeking Senior Clinical Research Associates I & II to join our FSP team in a remote capacity. You will partner with a sponsor to oversee oncology trials, ensuring data integrity, patient safety, and regulatory compliance across investigative sites.

As a study-level monitor, you will manage protocols from site activation to closeout, collaborate with site personnel and cross-functional teams, and help drive enrollment goals while maintaining high-quality study delivery in

Qualifications

• Bachelor's degree or RN qualification required.
• Minimum of 5 years oncology clinical research experience including monitoring.
• Strong knowledge of ICH GCP guidelines and trial regulations.
• Experience with CTMS and trial systems; proficient in English.

Responsibilities

• Lead monitoring activities for assigned oncology sites in line with the monitoring plan.
• Support site initiation, activation, and first subject visits readiness.
• Drive patient enrollment by maintaining site communications and addressing recruitment challenges.
• Ensure protocol, regulatory, and sponsor processes are followed throughout the trial lifecycle.
• Conduct onsite and remote monitoring visits with source data verification to ensure data quality.

Skills

Clinical monitoring

Site management

Relationship building

CTMS experience

Virtual monitoring

Oncology trials

English proficiency

Education

Bachelor's degree or RN qualification

Tools

CTMS

EDC systems

Electronic investigator systems

Job description

Parexel International is seeking Senior Clinical Research Associates I & II to join our FSP team in a remote capacity. You will partner with a sponsor to oversee oncology trials, ensuring data integrity, patient safety, and regulatory compliance across investigative sites.

As a study-level monitor, you will manage protocols from site activation to closeout, collaborate with site personnel and cross-functional teams, and help drive enrollment goals while maintaining high-quality study delivery in