Senior Clinical Research Associate
AL Solutions is seeking a highly experienced Senior Clinical Research Associate to join their global CRO clients. As a Senior CRA, you will play a key role in monitoring and managing clinical trials to ensure adherence to protocols, regulations, and quality standards. You will have the opportunity to work on a variety of studies and contribute to the advancement of medical research.
Key Responsibilities:
- Conduct site initiation, monitoring, and close-out visits at clinical investigator sites
- Review and evaluate study data, source documents, and case report forms for completeness, accuracy, and GCP compliance
- Identify protocol deviations and provide guidance to sites for corrective actions
- Ensure sites maintain adequate study supplies and investigational products
- Provide training and oversight to site staff on protocol requirements and GCP compliance
- Serve as the main point of contact for site staff regarding study conduct
- Review and approve monitoring reports and follow up on action items
- Collaborate with project teams to ensure successful study execution and data quality
- Participate in the selection and evaluation of new investigator sites
- Assist in feasibility assessments and budget/contract negotiations for new studies
- May act as a lead CRA, providing oversight and mentorship to junior CRAs
Requirements
– Bachelor’s degree in a life sciences-related field
– Minimum of 3 years’ experience as a CRA
– Solid knowledge of GCP and regulatory requirements
– Strong organizational and communication skills
– Ability to work independently and manage multiple priorities
Benefits
– Competitive salary
– competitive benefits
– Car allowance OR company car
– Career development opportunities
– Fully remote working
Whatever your career goals, my client is here to ensure you get there! If you are an experienced CRA looking for a new and exciting opportunity with the a lot of room for career progression then please get in touch! To apply, please submit your resume at: