Senior Clinical Research Coordinator
4 days ago
Are you a dedicated and compassionate individual with a passion for patient advocacy? We are seeking a Senior Clinical Research Coordinator to join our team at Guy's and St Thomas' NHS Foundation Trust.
About the RoleThis is an exciting opportunity to work in a dynamic and collaborative environment where you will play a key role in coordinating research clinics, organizing study-related care, and implementing strategies to identify and assist research participants.
You will be responsible for leading a portfolio of research studies, performing clinical assessments, and communicating proactively with study and clinical teams to ensure good participant experience and adherence to study protocols.
As a Senior Clinical Research Coordinator, you will also be expected to act as a mentor and support for new and junior team members, contribute to quality assurance processes within the team, and ensure the well-being of participants by adhering to study protocols, relevant regulations, and local Standard Operating Procedures (SOPs).
We are looking for someone who is highly organized, has excellent communication skills, and is able to work effectively in a fast-paced environment.
The estimated salary for this position is £40,000-£50,000 per annum, depending on experience.
Responsibilities- Provide excellent customer care skills to ensure patients and participants come first.
- Work within relevant regulations and ICH GCP ensuring that the clinical trial protocol is adhered to at all times.
- Lead on a portfolio of trials and coordinate participation, liaising with the clinical team to organize and ensure that trial-specific investigations are undertaken according to the protocol.
- Devise, implement, and evaluate strategies for recruiting participants into clinical studies and identifying individuals potentially eligible for research studies.
- Organize and facilitate participant appointments and follow-up phone calls.
- Accurately perform and record observations of clinical activities required according to personal competencies and the study protocol.
- Report any adverse events or health concerns which occur whilst the participant is taking part in the study to the appropriate doctor or nurse in a timely manner.
- Liaise with pharmacy to co-coordinate the availability and dispensing of study drugs if appropriate.
- Perform tasks requiring clinical and laboratory skills, including phlebotomy, venepuncture, tissue, and blood sample preparation within clinic and laboratory in line with personal competencies and approved study protocol.
- Process biological samples according to personal competencies and the study-specific protocol and laboratory manual.
- Provide ongoing support to the participant and carer whilst participating in the clinical study.
- Communicate study-related information effectively with the research team and study participants and their family members.
- Engage effectively with other departments and wards at the site/s to promote a good working environment, integration of research, and open channels of communication.
- Strong organizational and time management skills.
- Excellent communication and interpersonal skills.
- Ability to work effectively in a fast-paced environment.
- High level of discretion and confidentiality when dealing with sensitive information.
- Good knowledge of clinical research principles and procedures.
- Ability to work independently and as part of a team.
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