Role: Principal Investigator / Clinical Research Physician
Company: Site Management Organisation
Location: Birmingham / On-site
Apsida are currently recruiting on behalf of a well-funded & highly progressive Site Management Organisation in Europe. This company have gone from strength to strength over the past few years and are in a fanatics stage of growth.
You will be given the opportunity to take ownership of your responsibilities while also working in an experienced team that can positively impact your career development.
Responsibilities
- Conduct clinical trials according to the protocol, regulatory requirements, and ethical standards
- You will be responsible for managing the overall conduct of the study, including the safety of study participants, retention and recruitment
- Ensure that all study-related documents are completed accurately and in a timely manner
- Ensure that the study site is in compliance with all applicable regulations and guidelines
- Provide mentorship and training to study team members
- Act as the primary point of contact for the sponsor and regulatory authorities
Requirements
- Medical degree or equivalent
- GMC registered
- Experience in conducting clinical trials in compliance with regulatory requirements and ethical standards
- Knowledge of ICH-GCP guidelines and other applicable regulations and guidelines
- Strong communication and leadership skills
- Ability to work independently and collaboratively as part of a team
- Good organizational and time management skills
I’m looking to put a shortlist together for this client, to highlight your interest please send your CV or an email to sam.rodriguez@apsida.co.uk
Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK) & Boston (USA) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost effective, high quality and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.
