Principal Clinical Research Associate

RBW Consulting; Greater London; Remote; GBP 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a Principal Clinical Research Associate to join their dynamic team. This exciting role offers the opportunity to manage investigator sites throughout the study life cycle, from start-up to close-out, while working on innovative CAR-T and Gene Therapy studies. The company prides itself on its commitment to advancing clinical research and improving patient outcomes. With a focus on regional travel and multiple promotion opportunities, this position promises a fulfilling career path in a supportive and inclusive environment. If you're passionate about clinical operations and eager to make a difference, this role is perfect for you.

Qualifications

• 4+ years of proven CRA experience in clinical research.
• Broad knowledge of medical terminology and patient management.

Responsibilities

• Manage investigator sites through the study life cycle from start-up to close-out.
• Conduct feasibility, initiation, monitoring, and closeout visits for research sites.

Skills

Clinical Research Associate (CRA) experience

Knowledge of medical terminology

Patient management

Drug therapy techniques

Clinical research methodologies

Education

Bachelor of Science in health-related field

Job description

Direct message the job poster from RBW Consulting

Principal Recruitment Consultant | Clinical Operations | Global Recruitment

• Job Title: Principal Clinical Research Associate
• Location: Remote with regional travel
• Company: Global CRO

RBW Consulting are excited to announce an opportunity on behalf of one of our close clients. This company is a renowned CRO with leading healthcare intelligence and a European culture. They treat unmet disease target areas and advance clinical research by providing outsourced services to pharmaceutical and biotechnology companies.

Here, you can travel regionally, earn increased reduced travel in the position, and have up to 4 promotion & salary increase opportunities throughout the year. Not only this but you can work on interesting CAR-T and Gene Therapy studies.

Key accountabilities

• Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out);
• Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
• Prepare accordingly and attend investigator meetings, coordinating timely delivery and subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues;
• Perform source document verification and case report form review;
• Perform regulatory document review;
• Perform adverse event and serious adverse event reporting and follow-up; and
• Assess patient recruitment and retention.

Qualifications

• Bachelor of Science in health-related field (or equivalent)
• Proven CRA experience; 4 years minimum
• Broad knowledge of medical terminology and clinical patient management
• Basic knowledge of drug therapy techniques and clinical research methodologies

To apply:

Please click ‘apply’ or contact Joe Pearce for any further information

About RBW Consulting

RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients. We give back by playing an active role in funding initiatives that change lives. We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.

We are an equal opportunities Recruitment Business and Agency

RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.

Seniority level

• Associate

Employment type

• Full-time

Job function

• Health Care Provider, Research, and Quality Assurance
• Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Staffing and Recruiting