Job Description
MediCore Solutions is seeking a highly skilled Senior Clinical Research Associate to join our dynamic team in London. As a leader in the pharmaceutical and biotechnology sectors, we are dedicated to accelerating the development of life-saving therapies. In this pivotal role, you will oversee clinical trials from initiation to close-out, ensuring the highest standards of data integrity and regulatory compliance.
We offer a competitive benefits package, including a hybrid working model, continuous professional development, and a culture that values innovation and compassion. If you are driven by the challenge of managing complex clinical studies and want to make a tangible impact on global health, we want to hear from you.
Key Benefits:
- Competitive salary and performance bonus structure.
- Hybrid working flexibility.
- Comprehensive health, dental, and life insurance.
- Professional certification sponsorship (GCP).
- Generous pension scheme and wellness allowance.
Responsibilities
- Manage the full lifecycle of clinical trials, including site initiation, monitoring, and close-out.
- Conduct on-site monitoring visits to ensure trial conduct aligns with protocol and Good Clinical Practice (GCP).
- Monitor data quality, integrity, and completeness across clinical databases.
- Communicate effectively with cross-functional teams, including clinical operations, data management, and medical affairs.
- Ensure compliance with local and international regulatory requirements and sponsor Standard Operating Procedures (SOPs).
- Resolve trial-specific issues and implement corrective and preventive actions (CAPAs).
- Train and mentor junior staff and Site Investigators to foster a collaborative environment.
Qualifications
- Minimum of 2-4 years of experience in clinical research or a related field.
- Bachelor’s degree in Nursing, Life Sciences, Pharmacy, or a related field.
- Current GCP certification (e.g., ECP or ACRP) is required; certification preferred.
- Strong knowledge of ICH-GCP guidelines, FDA regulations, and local health authority requirements.
- Excellent interpersonal and communication skills, with the ability to influence stakeholders at all levels.
- Proficiency in using electronic data capture (EDC) systems (e.g., Medidata Rave, Oracle Clinical) and MS Office suite.
- Ability to travel up to 50% within the UK and Europe.