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- Tasks: Lead clinical studies, ensuring patient safety and compliance with regulations.
- Company: Join Thermo Fisher Scientific, a leader in making the world healthier and safer.
- Benefits: Enjoy a standard Monday to Friday schedule with a supportive team environment.
- Why this job: Make a real impact on patients' lives while advancing your career in clinical research.
- Qualifications: Must be a GMC registered doctor with clinical research experience preferred.
- Other info: Be part of a diverse team that values integrity, innovation, and collaboration.
The predicted salary is between 36000 - 60000 £ per year.
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life – To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.
Alongside clinical research through our PPD clinical research portfolio, our work in Accelerated Enrollment Solutions optimizes each step of the patient journey in clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on – now and in the future.
Are you a GMC registered Doctor who is interested in working in the dynamic clinical research industry? Are you passionate about improving patients' lives for the better? We are currently looking to recruit a Clinical Research Physician for our Synexus Clinical Research site in Birmingham, United Kingdom. Working days, Monday to Friday, 37 hours a week, the main priority will always be patient safety.
Key responsibilities for a Clinical Research Physician are as follows:
- Carries out clinical evaluation and assessment of participants to ensure eligible participants are recruited and monitored for safety and adherence.
- Acts as Principal Investigator (PI) or Co-Investigator for studies, ensuring compliance with ICH/GCP and local regulations.
- Attends Site Initiation Visits (SIV), Pre-Selection Visits (PSV), and Investigator meetings as required.
- Participates in recruitment initiatives and strategy development to ensure targets are achieved; ensuring recruiting studies enroll according to plan within timelines and targets.
- Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants.
- Interprets protocols and Investigator's Brochure (IB).
- Manages and reviews IVRS, CRF/EDC, if applicable.
- Oversees management of investigational medical product (IMP).
- Oversees multiple studies and/or studies with higher numbers.
- Completes documentation for PI handover.
- Cares for and protects the safety of participants through ethical conduct; this should receive the highest priority at all times during all aspects of the study.
- Fulfills and complies with all medical duties, ensuring clinical trials are performed to acceptable medical, scientific, and ethical standards and meet the requirements as per protocol, SOP/COP, ICH, and local GCP guidelines and regulations.
To be considered for this opportunity, you will require the following skills and experience:
- Be a GMC registered doctor with no limitations to practice.
- Ideally, some previous experience within clinical research.
- Have working knowledge of GCP (ICH/GCP and local regulations compliance).
- Demonstrate the inclination to provide practical help and guidance to colleagues, providing practical solutions for problems and supporting their development.
- Show meticulous attention to detail in recording patient information and data, ensuring queries are acted upon in a timely and efficient manner.
- Be a team player, capable of building and sustaining positive relationships with colleagues as well as patients.
Our Mission is to enable our customers to make the world healthier, cleaner, and safer.
Research Physician II employer: Thermo Fisher Scientific Inc.
Contact Detail:
Thermo Fisher Scientific Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Research Physician II
✨Tip Number 1
Familiarise yourself with the latest developments in clinical research and ICH/GCP guidelines. This will not only help you during interviews but also demonstrate your commitment to patient safety and ethical standards, which are crucial for the role.
✨Tip Number 2
Network with professionals already working in clinical research. Attend relevant conferences or webinars to connect with others in the field. This can provide insights into the industry and may even lead to referrals for job openings.
✨Tip Number 3
Prepare to discuss your previous experiences in clinical settings, especially any roles where you acted as a principal investigator or co-investigator. Highlight specific examples of how you ensured compliance with regulations and improved patient outcomes.
✨Tip Number 4
Showcase your teamwork skills by preparing examples of how you've collaborated with colleagues in past roles. Emphasising your ability to build positive relationships will resonate well with the values of Thermo Fisher Scientific.
We think you need these skills to ace Research Physician II
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of a Research Physician II. Familiarise yourself with clinical research protocols, ICH/GCP guidelines, and the specific duties mentioned in the job description.
Tailor Your CV: Customise your CV to highlight relevant experience in clinical research and your GMC registration. Emphasise any previous roles where you acted as a Principal Investigator or Co-Investigator, and showcase your attention to detail and teamwork skills.
Craft a Compelling Cover Letter: Write a cover letter that reflects your passion for improving patient lives and your commitment to ethical conduct in clinical trials. Mention specific experiences that demonstrate your ability to meet the key responsibilities outlined in the job description.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for any spelling or grammatical errors, and ensure that all information is accurate and clearly presented. A polished application reflects your professionalism and attention to detail.
How to prepare for a job interview at Thermo Fisher Scientific Inc.
✨Understand the Role and Responsibilities
Before the interview, make sure you thoroughly understand the key responsibilities of a Research Physician II. Familiarise yourself with clinical research protocols, ICH/GCP guidelines, and the specific duties mentioned in the job description. This will help you articulate how your experience aligns with their needs.
✨Showcase Your Clinical Experience
Be prepared to discuss your previous clinical experience, especially any work related to clinical trials or research. Highlight specific examples where you ensured patient safety and adhered to ethical standards, as this is crucial for the role.
✨Demonstrate Teamwork and Communication Skills
Since the role requires collaboration with colleagues and patients, be ready to provide examples of how you've successfully worked in teams. Discuss how you communicate effectively with both medical staff and participants to ensure smooth operations in clinical settings.
✨Prepare Questions About Patient Safety and Ethics
During the interview, ask insightful questions about how the company prioritises patient safety and ethical conduct in their studies. This shows your commitment to these values and helps you gauge if the company's culture aligns with your own professional ethics.
