Early Phase Clinical Research Physician

Greater Manchester, England, United Kingdom

4/17/2025

We are seeking to appoint a Clinical Research Physician – level 1 (CRP1) to join our dedicated team at our Early Phase Unit in Manchester. 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.

We welcome applications from newly qualified doctors with 2 years of experience (FY 1&2 included) and no prior experience in clinical research. This is an ideal opportunity for candidates exploring an alternative to NHS or private sector

.
If you have prior experience in research or you have a real interest in changing to a career in clinical research and bring additional years of experience, then we would like to hear from you to

o!
Starting salary: £50,

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

ls)
General shift work includes some weekends (on rotat

ion)
KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUI

RED: Esse

• ntialFull and current GMC registr
• ation2 years post-graduation experience (manda

tory)Desi

• rable2+ Years of UK clinical experience in any spec
• ialtyPrevious clinical research experience in SM
• O/CROPharmaceutical experience 0-2 years (desir
• able)MRCP /MRCGP (desir

able)
RESPONSIBILI

TIES: Clinical activ

• ities:Fulfil the role of Sub Investigator / Principal Investigator where dele
• gated.Provision of medical care and oversight of clinical trial partici
• pants.Ensure trial related procedures are completed in accordance with ICH-GCP guidelines and in compliance with the pro
• tocol.Review medical records of potential study partici
• pants.Remain proactive in participants study visits, including taking informed consent, physical examinations and other clinical proce
• dures.Ensure that study documentation is completed, signed off, and actioned, as approp
• riate.Maintain accurate source
• notes.Review medical reports and lab re
• sults.Assist clinical staff members in various clinical activities as req
• uired.Participate in site monitoring visits with Clinical Research Assoc
• iates.Ensure timelines for data queries are ach
• ieved.Continuously work towards maintaining and improving quality in all
• areas.On-call rota duties as req
• uired.Assess and review memory clinic patients (only applicable to sites where MAC operates a memory c

linic)
Mana

• gement:Attend Investigator Meetings (IM), Site Initiation Visits (SIV) and Pre-Study Selection Visits (PSSV) as re
• quired.Review source doc
• uments.Participate in sponsor and regulatory audits as re
• quired.Participate in meetings with colleagues and cus

tomers.
Le

• adershipProvide practical help and guidance to othe
• r staff.Instil confidence in patients, customers and col
• leagues.Providing training to the clinical/ recruitment teams on essential medical information and protocols when r

equired.
Commercial Awareness and Contribution t

• o TargetsMaintain an awareness of our key customers and market com
• petitors.Share ideas from previous work environments to enhance curr
• ent role.Maintain an awareness of site KPI’s and contribute positively to meeting these

targets.
Professional d

• evelopmentAlways maintain a professional attitude and appearance to customers/c
• olleagues.Ensure that GMC requirements for revalidation are met appropriately to retain license to
• practice.Identify opportunities for self-de

velopment.
R

• ecruitment: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 correct
• ive action.Keep up to date with study status, ensuring each stage is
• optimised.Establish and maintain relationships with local GPs, Consultants and service

provide

• rs.
  General:Share experience and knowledge with colleagues as appropriate and in an appropr
• iate manner.Compliance with MAC policy on equality a
• nd diversityTo maintain professional qualifications required for the role, including continuous personal
• developmentTo work to the requirements of SI 2004 no 1031 and amendments thereof, which includes Good Clini
• cal PracticeTo work according to MAC SOPs, guidelines
• and policiesTo work according to current data protection standards and practice good information management. Maintenance of strict confidentiality of patient and business-r
• elated 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 outTo support the aims of MAC and to represent MAC appropriately in a professional way to all o

ur customers
PHYSICAL, WORK ENVIRONMENT, TR

• AVEL DEMANDS:Dealing with b
• odily fluids.Long periods looking at a com
• puter screen.Meeting deadlines and working within stri
• ct timelines.Ability to travel between sites
• if required.Ability to travel to national/internatio

nal meeti

• ngs.
  BENEFITS:Competitive salary in keeping with pharmaceutical industry standards and will refl
• ect experienceOpportunities to enrol in higher medical training programme
• s such as PMSTHe
• alth InsuranceFree
• onsite parking25 days annual leave (increasing in increments to 30 days after 6 y
• ears' service)Your bir

thday off work
MAC Clinical Research invites applications from highly motivated candidates, with a desire to fulfil their full potential. You will be working with an organisation that sees you as an investment and is keen for you to achieve your care

er aspirations.
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 reque

st as necessary.