Clinical Research Physician (Internal Only)

  • Mon-Fri
  • Medics
  • Leeds

Description

We are seeking to appoint a CRP1 (Clinical Research Physician – level 1) to join our dedicated team at our clinic in Leeds, West Yorkshire. The focus of this role is to fulfil the role of Sub-Investigator and Principal Investigator (where delegated) in clinical research studies in compliance with the protocol and ICH/GCP. 



Starting salary: £50,000

(additional considerations will be made for those that match some/all of the "desirable" criteria outlined in Key Skills)

Requirements

Essential 

  • UK GMC Registered with valid licence to practice
  • 2 years post graduate experience of working as a doctor in the UK within the NHS (minimum)

Desirable 

  • 2+ Years of UK clinical experience in any specialty
  • 2+ years of psychiatry experience
  • Previous clinical research experience in SMO/CRO

 

RESPONSIBILITIES:  

Clinical activities: 

  • Fulfil the role of Sub Investigator / Principal Investigator where delegated. 
  • Provision of medical care and oversight of clinical trial participants. 
  • Ensure trial related procedures are completed in accordance with ICH-GCP guidelines and in compliance with the protocol. 
  • Review medical records of potential study participants. 
  • Remain proactive in participants study visits, including taking informed consent, physical examinations and other clinical procedures. 
  • Ensure that study documentation is completed, signed off, and actioned, as appropriate. 
  • Maintain accurate source notes. 
  • Review medical reports and lab results. 
  • Assist clinical staff members in various clinical activities as required. 
  • Participate in site monitoring visits with Clinical Research Associates. 
  • Ensure timelines for data queries are achieved. 
  • Continuously work towards maintaining and improving quality in all areas. 
  • On-call rota duties as required. 
  • Assess and review memory clinic patients (only applicable to sites where MAC operates a memory clinic) 

Management: 

  • Attend Investigator Meetings (IM), Site Initiation Visits (SIV) and Pre-Study Selection Visits (PSSV) as required. 
  • Review source documents. 
  • Participate in sponsor and regulatory audits as required. 
  • Participate in meetings with colleagues and customers. 

 

Leadership 

  • Provide practical help and guidance to other staff. 
  • Instil confidence in patients, customers and colleagues. 
  • Providing training to the clinical/ recruitment teams on essential medical information and protocols when required. 

 

Commercial Awareness and Contribution to Targets 

  • Maintain an awareness of our key customers and market competitors. 
  • Share ideas from previous work environments to enhance current role. 
  • Maintain an awareness of site KPI’s and contribute positively to meeting these targets. 

 

Professional development 

  • Always maintain a professional attitude and appearance to customers/colleagues. 
  • Ensure that GMC requirements for revalidation are met appropriately to retain license to practice. 
  • Identify opportunities for self-development. 


Recruitment: 

  • Assist with the development of recruitment strategy with the Envision team as a therapy area specialist. 
  • Maintain awareness of chat and screen fails and patient drop-out rates, taking appropriate corrective action. 
  • Keep up to date with study status, ensuring each stage is optimised. 
  • Establish and maintain relationships with local GPs, Consultants and service providers. 

  

General: 

  • Share experience and knowledge with colleagues as appropriate and in an appropriate manner. 
  • Compliance with MAC policy on equality and diversity 
  • To maintain professional qualifications required for the role, including continuous personal development 
  • To work to the requirements of SI 2004 no 1031 and amendments thereof, which includes Good Clinical Practice 
  • To work according to MAC SOPs, guidelines and policies 
  • To work according to current data protection standards and practice good information management. Maintenance of strict confidentiality of patient and business-related data. 
  • To maintain a high level of initiative and personal responsibility, liaising appropriately with team members and managers to ensure your job role is efficiently carried out 
  • To support the aims of MAC and to represent MAC appropriately in a professional way to all our customers 

 

PHYSICAL, WORK ENVIRONMENT, TRAVEL DEMANDS: 

  • Dealing with bodily fluids. 
  • Long periods looking at a computer screen. 
  • Meeting deadlines and working within strict timelines. 
  • Ability to travel between sites if required. 
  • Ability to travel to national/international meetings. 

Benefits

  • Competitive salary in keeping with pharmaceutical industry standards and will reflect experience 
  • Opportunities to enrol in higher medical training programmes such as PMST
  • Health Insurance 
  • Free onsite parking 
  • 25 days annual leave (increasing in increments to 30 days after 6 years' service) 
  • Your birthday off work 


Please email [email protected] should you require any special arrangements or reasonable adjustments to be made throughout this selection process. This will enable us to accommodate your request as necessary.