Opportunity at
Precision Medicine GroupClinical Research Associate II/ Senior Clinical Research Associate
Precision Medicine Group is seeking a Clinical Research Associate II or Senior Clinical Research Associate to join its team on a fully home-based basis in the…
Career Tools
About This Role
Precision Medicine Group is seeking a Clinical Research Associate II or Senior Clinical Research Associate to join its team on a fully home-based basis in the UK or Northern Ireland. The organization operates as a specialized contract research organization focused on oncology and rare diseases, combining advanced biomarkers, data analytics, and adaptive clinical trial designs to advance cancer therapies. This position is suited for a professional who thrives in a…
Job Description
Precision Medicine Group is seeking a Clinical Research Associate II or Senior Clinical Research Associate to join its team on a fully home-based basis in the UK or Northern Ireland. The organization operates as a specialized contract research organization focused on oncology and rare diseases, combining advanced biomarkers, data analytics, and adaptive clinical trial designs to advance cancer therapies.
This position is suited for a professional who thrives in a collaborative environment with manageable protocol loads, reasonable travel expectations, and direct support from line management. Employees benefit from a smaller organization structure where individual contributions influence projects and professional growth.
The person in this role will oversee clinical study progress at investigative sites, manage study setups, and ensure compliance with protocols, standard operating procedures, ICH-GCP guidelines, and relevant regulations. Responsibilities include coordinating investigator identification, helping prepare regulatory submissions, and conducting pre-study, initiation, and monitoring visits.
Responsibilities
- Monitor and manage the progress of clinical studies at investigative sites
- Ensure clinical studies adhere to study protocols, standard operating procedures, ICH-GCP, and all applicable standards
- Coordinate site setup and monitoring activities including identifying investigators
- Assist with the preparation of regulatory submissions
- Conduct pre-study and study initiation visits
- Identify potential study risks and propose mitigation strategies
Requirements
- More than one year of clinical research associate experience within a contract research organization or the pharmaceutical industry
- Oncology experience
- Availability for domestic travel including overnight stays of approximately 50 to 60 percent
- Fluency in English
- Legal authorization to work in the country of employment without employer sponsorship
Qualifications
- Four-year college degree or equivalent experience
- Phase I experience
- First-In-Human experience
- Ability to conduct international travel for senior-level positions
Core Skills
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
Where is this job located?
This position is fully home-based and can be performed from the UK or Northern Ireland.
What level of travel is required for this role?
Domestic travel, including overnight stays, may require a commitment of approximately 50 to 60 percent, with international travel potentially required for senior-level positions.
What experience is necessary to qualify?
Candidates must have more than one year of CRA experience within a CRO or the pharmaceutical industry, along with essential oncology experience and fluency in English.
What is the salary for this position?
The job posting does not specify a salary.
Sample Interview Questions
AI-generated questions tailored to this specific role — a preview of the full practice set.