Description review
Clinical Trial Manager (Oncology) - UK (Home-based) - FSP
Parexel · United Kingdom · back to the listing
HR standards
60/100
needs work
Title ↔ description
84/100
solid
Reads as
Project Manager
86% confident
What this role officially is
project manager — ESCO, the EU occupation classification
Project managers ensure that a project is completed on time, within budget, and that its objectives are met. They oversee the project, manage the team, ensure the most efficient resources are used and ensure that all parties involved are satisfied.
Also known as: project coordinator, project leader, special project manager, project expediter, senior project manager, project director
How others title the same work
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What the listing never says
- 25 bullet points. Long requirement lists deter qualified candidates, who read them as hard gates. Scope clarity
- No pay range published. Candidates cannot tell whether applying is worth their time. Pay transparency
The listing, marked up
Nothing in the wording of this listing tripped a check. The scores above still judge how complete and coherent it is.
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
About Parexel
Parexel is a leading global clinical development partner delivering insights‑driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient‑focused clinical trials that broaden access and make research a care option for anyone, anywhere.
We work with focus, agility, and shared purpose – moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry‑leading innovation, With Heart®.
About the Role
We are seeking a Clinical Trial Manager (CTM) to join our team in a remote capacity in the UK. As a CTM, you will act as a member of the sponsor’s Development Operations team and will manage individual clinical trials and/or programs as part of their Clinical Trial Working Group.
You’ll join a fast‑paced, growth‑oriented environment focused on making a meaningful impact through the set-up, execution and delivery of assigned trials and contribute to delivery of the sponsors pipeline through accurate planning and efficient execution of trials that bring speed and value to participating subjects and sites.
With diverse teams and continuous learning opportunities, the Clinical Trial Manager can explore career paths and expand skills across clinical research.
Key Responsibilities
• Manage external vendors and contract research organisations.
• Prepare study documents such as the Monitoring Manual, Study Operations Manual, Source Data Verification Plan and Laboratory Manual.
• Coordinate and be responsible for the design of study materials such as CRFs, patient diaries, study participation cards and source documents.
• Assist with protocol development and study report completion.
• Manage monitoring activities (may include routine on-site clinical monitoring) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study protocols.
• Provide guidance, direction, and management to CRAs.
• Track patient enrollment; qualify, initiate, monitor, perform closeout activities, and review site reports; and assist in coordination of data management activities.
· Coordinate study supplies.
• Negotiate contracts with vendors of clinical trial services.
• Review Informed Consent Forms, CRFs, and study related materials.
• Plan and participate in investigator meetings.
• Assist and support data query process.
• Assure regulatory compliance of investigational sites with sponsor’s SOPs and FDA and ICH guidelines.
• Ensures trial master file is current and maintained.
Please note that responsibilities may require a work schedule that may include working outside of “normal” work hours, to meet business demands.
Candidate Profile
You’ll thrive in this role if you bring:
• Experience in clinical trial project management, preferably across international trials.
• The ability to collaborate across teams and communicate clearly.
• A patient‑focused mindset and strong attention to detail.
Required Qualifications
• Bachelor’s, nursing degree or equivalent required, science preferred.
• 5 or more years of industry experience in clinical studies (Pharmaceutical, Biotech or CRO).
• Proven track record with relevant clinical trials experience, including strong performance as a CRA in the pharmaceutical industry (i.e. biotechnology, pharmaceutical, CRO, medical device).
• Proven experience of clinical trial management.
• Proven management/leadership of people in a matrixed environment.
• Demonstrated working knowledge of GCP, ICH guidelines and regulations, regulatory requirements, and clinical trial processes.
• Demonstrated ability to work independently and in a team environment.
• Proficiency with MS Office (e.g. Word, Excel, PowerPoint, Outlook).
• Excellent oral and written communication skills and strong organisational abilities.
If this job doesn’t sound like the next step in your career, but perhaps you know of someone who’d be a perfect fit, send them the link to apply!
We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.
Originally posted on Himalayas
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
About Parexel
Parexel is a leading global clinical development partner delivering insights‑driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient‑focused clinical trials that broaden access and make research a care option for anyone, anywhere.
We work with focus, agility, and shared purpose – moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry‑leading innovation, With Heart®.
About the Role
We are seeking a Clinical Trial Manager (CTM) to join our team in a remote capacity in the UK. As a CTM, you will act as a member of the sponsor’s Development Operations team and will manage individual clinical trials and/or programs as part of their Clinical Trial Working Group.
You’ll join a fast‑paced, growth‑oriented environment focused on making a meaningful impact through the set-up, execution and delivery of assigned trials and contribute to delivery of the sponsors pipeline through accurate planning and efficient execution of trials that bring speed and value to participating subjects and sites.
With diverse teams and continuous learning opportunities, the Clinical Trial Manager can explore career paths and expand skills across clinical research.
Key Responsibilities
• Manage external vendors and contract research organisations.
• Prepare study documents such as the Monitoring Manual, Study Operations Manual, Source Data Verification Plan and Laboratory Manual.
• Coordinate and be responsible for the design of study materials such as CRFs, patient diaries, study participation cards and source documents.
• Assist with protocol development and study report completion.
• Manage monitoring activities (may include routine on-site clinical monitoring) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study protocols.
• Provide guidance, direction, and management to CRAs.
• Track patient enrollment; qualify, initiate, monitor, perform closeout activities, and review site reports; and assist in coordination of data management activities.
· Coordinate study supplies.
• Negotiate contracts with vendors of clinical trial services.
• Review Informed Consent Forms, CRFs, and study related materials.
• Plan and participate in investigator meetings.
• Assist and support data query process.
• Assure regulatory compliance of investigational sites with sponsor’s SOPs and FDA and ICH guidelines.
• Ensures trial master file is current and maintained.
Please note that responsibilities may require a work schedule that may include working outside of “normal” work hours, to meet business demands.
Candidate Profile
You’ll thrive in this role if you bring:
• Experience in clinical trial project management, preferably across international trials.
• The ability to collaborate across teams and communicate clearly.
• A patient‑focused mindset and strong attention to detail.
Required Qualifications
• Bachelor’s, nursing degree or equivalent required, science preferred.
• 5 or more years of industry experience in clinical studies (Pharmaceutical, Biotech or CRO).
• Proven track record with relevant clinical trials experience, including strong performance as a CRA in the pharmaceutical industry (i.e. biotechnology, pharmaceutical, CRO, medical device).
• Proven experience of clinical trial management.
• Proven management/leadership of people in a matrixed environment.
• Demonstrated working knowledge of GCP, ICH guidelines and regulations, regulatory requirements, and clinical trial processes.
• Demonstrated ability to work independently and in a team environment.
• Proficiency with MS Office (e.g. Word, Excel, PowerPoint, Outlook).
• Excellent oral and written communication skills and strong organisational abilities.
If this job doesn’t sound like the next step in your career, but perhaps you know of someone who’d be a perfect fit, send them the link to apply!
We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.
Originally posted on Himalayas