Precision Medicine Group · Remote, United Kingdom

Senior Clinical Research Associate

最近核查時仍有刊登最近確認刊登:2026-11-06 18:32:37.675507+00

招聘狀態可能變動,申請前請查看原始職位。

薪酬未公開
學歷未说明
語言英语 · 未指定等级
經驗Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment

來源發布日期:2026-09-21T10:25:02-04:00

職位要求

  • You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
  • Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
  • Fluency in English and the local language is required
  • Candidates must be legally authorized to work in the country of employment without employer sponsorship.

原文資格條件

以下摘錄自招聘來源,適用條件請以原文為準。

  • Candidates must be legally authorized to work in the country of employment without employer sponsorship.
查看招聘來源的要求摘錄

原始資料於 2026-11-06T13:30:09.447379+00:00 查閱;內容可能已更新,請查看原始職位。

About you:
You are calm, thoughtful, and responsive when things don’t go as planned.
You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
You find quick and creative ways of overcoming difficulties.
You have an impeccable eye for detail.
You identify potential study risks and propose solutions on how to mitigate them.
You take responsibility in the quality and outcomes of your work.
You are adept at handling conflict by using tried and true resolution strategies.
How we will keep you busy and support your growth:
You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
Senior CRAs handle appropriately sized clinical trials, and support clinical study teams with trials that are larger in scope. You will also have the opportunity to train and mentor junior staff members. You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.
Qualifications:
Minimum Required:
4-year college degree or equivalent experience
Holder of CRA certificate
Other Required:
Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment
Experience monitoring clinical trials across a variety of therapeutic areas.
Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
Fluency in English and the local language is required
Additional language(s) will be considered an asset
Preferred:
Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
Study start up activities experience
For Senior CRAs, understanding of financial management
Why Precision for Medicine?
At Precision for Medicine, we combine the agility and collaboration of a specialized CRO with the scientific expertise needed to support innovative clinical development programmes. Our employees are empowered to make an impact, build meaningful client relationships, and grow their careers in an environment that values quality, accountability, and professional development.
Please note: This is an evergreen opportunity intended to build our network of experienced clinical research professionals for future project requirements. Hiring decisions and timelines will be dependent upon business needs and upcoming study opportunities.
Please, apply in English.
#LI-EK1 #LI-Remote
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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].
Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [contact details available on source] so we can investigate and take appropriate action.
Candidates must be legally authorized to work in the country of employment without employer sponsorship.

來源:公司官网 · 資料查閱日期 2026-11-06T13:30:09.447379+00:00。職位狀態及要求請以原始招聘頁面為準。