Principal Cloud Solutions Architect

The Investigator leads and oversees clinical trials at their site, ensuring participant safety, regulatory compliance, and high-quality data collection. They provide medical expertise, guide study teams, and communicate effectively with sponsors, study directors, and site staff., * Provide overall medical direction and review study protocols in line with GCP and investigational plans.

• Ensure participant safety, rights, and confidentiality throughout the trial.
• Oversee clinical procedures, assessments, and administration of investigational products.
• Ensure accurate, complete, and timely data collection; maintain proper documentation and regulatory compliance.
• Collaborate with clinical operations, research staff, sponsors, and IRBs, including reporting adverse events and protocol deviations.
• Review and monitor protocol adherence, study materials, and investigational product use.
• Facilitate monitoring, audits, and inspections by sponsors and regulatory authorities.
• Inform participants and IRBs appropriately if the trial is terminated or suspended., Principal Medical Writer, Clinical Development Our client is a Biotech company with a strong pipeline, now wish to hire a Principal Medical Writer within their Clinical Development team, working closely with functional teams e.g. Clinical Operations, Regulatory Affairs,..., The Senior Pricing Analyst will play a pivotal role in advancing the company's strategic objectives by enhancing their pricing and commercial capabilities. This role will support the Commercial Team and Proposition Team through proactive development and execution of the...

• Strong knowledge of GCP, regulatory requirements, and biomedical research ethics.
• Excellent communication, collaboration, and critical thinking skills.
• Attention to detail and dynamic problem-solving capabilities.
• Commercial understanding of business operations.
• Willingness to travel as required (up to 10%).

Education & Experience:

• Medical degree recognised by the GMC with an active GMC license.
• GCP training and certification.
• Board certification or eligibility in a specialty relevant to the research conducted at the site.