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- Tasks: Join our Medical team as a Clinical Research Physician managing Phase I and II clinical trials.
- Company: Be part of a dynamic medical organization in Nottingham focused on innovative research.
- Benefits: Enjoy competitive salary, additional remuneration for on-call duties, and opportunities for professional growth.
- Why this job: Make a real impact on volunteer welfare while gaining hands-on experience in clinical research.
- Qualifications: Must have a full license to practice, two years of clinical experience, and preferably ALS certification.
- Other info: This role includes an on-call rota and requires high concentration and adherence to safety procedures.
The predicted salary is between 43200 - 72000 £ per year.
We have a fantastic opportunity to join our Medical team in Nottingham as a Clinical Research Physician. As the Clinical Research Physician, you will be responsible for the medical aspects of Phase I and II clinical trials. Managing the process by which a volunteer is screened for a specific study to determine their eligibility to take part in the study and responsible for the everyday running of studies including the welfare of volunteers under the direction of the Principal Investigator.
Key responsibilities of a Clinical Research Physician include:
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To act as a medically qualified person responsible for medical aspects of Phase I and II activities
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To manage the process by which a volunteer is screened for a specific study, to determine their eligibility to take part in the study
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To take medical responsibility for the everyday running of studies including the welfare of volunteers under the direction of the Principle Investigator
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To liaise with the Principal Investigators, Lead Scientists and members of the study teams about any medical and/or safety issues arising from a study
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To support the corporate goals by working closely with the Medical Science, Business Development and Marketing Departments
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To comply & adhere to GXP guidelines and regulations as required of this role
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To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards
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Performing a full physical examination for each volunteer
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Conducting or assisting clinical staff in the conduct of other study specific screening activities
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Reviewing all information gathered at pre study visit and confirming volunteer’s eligibility to take part in a study by signing the CRF
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To assist the Senior Research Physician / Principal Investigator with ward duties.
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In the event of a medical emergency occurring during the course of a study, to assist the physician responsible for the study and the clinical staff with the management of the emergency as needed, or to take temporary responsibility for the other volunteers whilst the emergency is being dealt with
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To ensure the volunteers health and welfare takes priority
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Provide study specific training and support to the Operations team prior to, during and after study days (as appropriate to the study) in order to ensure efficient execution of the study and acquisition of quality data
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To work closely with the PI to understand the rationale for study design to facilitate the planning and delivery of individual studies
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Production/review of the protocol, volunteer information and consent form, safety summary and any other documentation in conjunction with the Principal Investigator and other relevant personnel
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Act as study physician on selected studies
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To support the Principal Investigator in discussions with clients
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To participate in the on-call rota once has sufficient experience
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Responsible for the development and implementation of Standard Operating Procedures as required.
This position involves an on-call rota, you will participate in on-call day and night, including weekends and weekday nights, once you have attained sufficient experience. This is a mandatory commitment and is included in the overall salary.
This position also involves overnight medical cover and weekend morning cover, when required. You will receive additional renumeration for this.
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A full license to practice by the General Medical Council
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A minimum of two years of postgraduate clinical experience which should normally involve direct patient care and experience of prescribing.
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ALS certification preferred but can be obtained in post
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Membership of a medical defence union to include work in the pharmaceutical industry
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A scientific qualification (e.g. BSc) and/or postgraduate medical or scientific diploma or degree (e.g. MSc, PhD, MD, MRCP, MRCPath) is desirable but not essential.
The job may involve the following:
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Very high concentration of work
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Strict and tight deadlines
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Having to juggle a range of tasks/issues simultaneously
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Working in a hazardous environment with high requirement to follow safety procedures
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Working outside normal working hours
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Needing to respond to client demands
Clinical Research Physician employer: Quotient Sciences
Contact Detail:
Quotient Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Physician
✨Tip Number 1
Familiarize yourself with the latest GXP guidelines and Good Clinical Practice (GCP) standards. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high-quality study data.
✨Tip Number 2
Network with professionals in the clinical research field, especially those who have experience in Phase I and II trials. Engaging with them can provide valuable insights and potentially lead to referrals or recommendations.
✨Tip Number 3
Stay updated on current trends and advancements in clinical research, particularly in the areas relevant to the studies you'll be managing. This will help you speak confidently about your expertise during discussions with the Principal Investigator and other team members.
✨Tip Number 4
Prepare to discuss your experience with emergency medical situations and how you've handled them in the past. This is crucial for the role, as you'll need to demonstrate your ability to prioritize volunteer welfare during studies.
We think you need these skills to ace Clinical Research Physician
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Clinical Research Physician position. Understand the key responsibilities and qualifications required, as this will help you tailor your application.
Highlight Relevant Experience: In your CV and cover letter, emphasize your clinical experience, especially any work related to Phase I and II clinical trials. Mention specific examples where you managed volunteer welfare or adhered to GCP standards.
Showcase Your Qualifications: Clearly list your medical qualifications, including your GMC license and any postgraduate degrees. If you have ALS certification or membership in a medical defense union, make sure to highlight these as well.
Tailor Your Cover Letter: Write a personalized cover letter that addresses how your skills and experiences align with the responsibilities of the Clinical Research Physician role. Mention your ability to work under pressure and manage multiple tasks, as these are crucial for this position.
How to prepare for a job interview at Quotient Sciences
✨Understand the Clinical Trial Process
Make sure you have a solid grasp of the phases of clinical trials, especially Phase I and II. Be prepared to discuss how you would manage volunteer screening and ensure their eligibility for studies.
✨Highlight Your Medical Experience
Emphasize your postgraduate clinical experience and any direct patient care roles you've held. Discuss specific examples where you've had to make critical medical decisions or manage emergencies.
✨Familiarize Yourself with GCP Guidelines
Since adherence to Good Clinical Practice (GCP) is crucial, be ready to talk about your understanding of these guidelines and how you have applied them in previous roles.
✨Showcase Team Collaboration Skills
This role requires close collaboration with Principal Investigators and study teams. Prepare examples that demonstrate your ability to work effectively in a team and communicate medical issues clearly.
