Skip to main content

Research Physician I

Location Glasgow, 英国 Job Id R-01299341 Job Type フルタイム Category 臨床開発 Remote すべてオンサイト
検索結果に戻る
前のジョブ 次の仕事
JOB DESCRIPTION

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

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 patient’s lives for the better?

We are currently looking to recruit a Clinical Research Physician for our Synexus Clinical Research site in Glasgow, United Kingdom     

Working days, Monday to Friday, 37 hours a week, the main priority will always be patient safety. Acting as the principal investigator (PI) or co-investigator for some or all of the studies at the site they have the responsibility for all sponsor research studies while also ensuring ICH/GCP and local regulations are met. 

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. 
  • Principle Investigator (PI) or Co Investigator for some or all of the studies at the site ensuring ICH/GCP and local regulations are met.
  • Attends Site Initiation Visits (SIV), Pre-Selections 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 enrolment progress, pre-screening and screening success rates, screen failure rates, safety and retention of participants. 
  • Interprets protocols and 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 that 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 exciting 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 any problems and supporting their development
  • Show meticulous attention to detail in recording patient information and data ensuring any 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. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Close the popup
img1
当社は、応募にあたり何らかのサポートが必要な候補者の方は詳細をご覧ください
詳細を見る

類似した求人の通知を受け取る

サインアップし、類似した求人アラートをEメールで受け取る

成功！類似した求人に登録しました 失敗！この求人にはすでに登録済みです 失敗！類似した求人に登録できませんでした

類似の仕事

おすすめが見つかりません

当社では、優れた閲覧体験を提供し、サイトトラフィックを分析し、コンテンツをパーソナライズするためにCookieを使用します。当社がCookieを使用する方法と、ユーザーが [Cookie設定] ページにアクセスしてCookieを制御する方法についてお読みください。当サイトの使用を続行した場合、Cookieの使用に同意したことになります。
クッキー設定
How would you rate your experience popup
キャリアサイトのクッキー設定
個人情報