Clinical Research Associate I

AbbVie; Maidenhead; On-site; GBP 30,000 - 45,000; Full time

Job summary

A global biopharmaceutical company in Maidenhead is seeking a Clinical Research Monitor to oversee clinical investigative sites for trial compliance. The successful candidate will be responsible for ensuring adherence to protocols, managing site interactions, and training personnel. A health-related tertiary qualification and clinical research monitoring experience are required. Strong analytical and interpersonal skills are essential. This position offers opportunities for professional growth within a leading firm committed to innovation and patient care.

Qualifications

• Experience in on-site monitoring of investigational drug/device trials required.
• Current knowledge of clinical research regulations and ICH/GCP Guidelines.
• Strong planning, organizational, and analytical skills.

Responsibilities

• Monitor clinical investigative sites to ensure protocol execution.
• Conduct site qualification, initiation, and monitoring visits.
• Ensure compliance with regulatory standards and quality of data.

Skills

Clinical research monitoring

Regulatory compliance

Analytical skills

Interpersonal skills

Education

Tertiary qualification in health-related field

Job description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

To enable AbbVie’s emergence as a world class R&D organization, the position anticipates and proactively solves study‑related clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol level execution of SMM deliverables involving start‑up, execution, and close‑out of studies.

• Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research.
• Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs) and business processes.
• Overviews the overall activities of site personnel over whom there is no direct authority and motivates/influences them to meet study objectives. Proactively manages the site and ensures action plans are put into place as needed to ensure compliance. Ensures regulatory inspection readiness at assigned clinical sites.
• Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow‑up for all safety events by site personnel.
• Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations.
• Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members.
• Manages investigator payments as per executed contract obligations. Negotiates investigator/hospital agreements with stakeholders. Maintain and complete own expense reports as per local and applicable guidelines.
• Identifies, evaluates and recommends new/potential investigators/sites on an ongoing basis. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.

Qualifications

• Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing) preferred.
• Clinically‑related experience in clinical research monitoring. Experience in on‑site monitoring of investigational drug or device trials is required.
• Current in‑depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials.
• Current in‑depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations.
• Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and follow work processes within the assigned function.
• Strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity. Ability to address study related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated. Ability to use functional expertise and exercise good judgment.
• Demonstrated business ethics and integrity.

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html