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Precision Medicine Group

Senior Clinical Research Associate/ Clinical Research Associate II

Work from homeNew this week

Remote role where the employee must remain based in a particular country.

United Kingdom only

Employer listed it 2 days ago · Found 9h ago

First listed 2 days ago.

Salary

Not stated

Location

United Kingdom only

Timezone

GMT

Contract

Full-time

Experience

Senior

Category

Other

This employer didn't state pay. Jobs like this usually pay around $125k–$205k a year, a typical range taken from 166 senior-level other roles on Nomaders that do state pay. It's a guide, not an offer.

Remote flexibility

Work from home

This is a remote role, but the employee must be based in United Kingdom. It is work from home rather than work from anywhere.

What the employer says

  • Source listing states candidate location: "Remote, United Kingdom, Remote (UK)"

What Nomaders makes of it

  • Residency required in United Kingdom
  • Payroll and tax are likely handled in that country only

The quotes above are the employer's own words; the reading is ours. Always check the original listing and employment terms before working from another country.

About the role

Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.

CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.

We are hiring a Senior Clinical Research Associate/ Clinical Research Associate II, this position will be fully home based working in the UK or Northern Ireland.

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.).

Qualifications:

Minimum Required:

4-year college degree or equivalent experience

Other Required:

Candidates should ideally have more than 1 years CRA experience within the CRO or pharmaceutical industry.

Oncology experience, early phase experience desirable although not essential.

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

Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.

Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.

We invite you to learn more about our growing organization serving our clients that are researching groundbreaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company.

Requirements

  • ·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.

Benefits

No benefits package published with this listing. Ask about it at first interview.

How to apply

  1. 1Check the flexibility label above, work from home, matches where you plan to live and work.
  2. 2Tailor your CV to the role at Precision Medicine Group, mentioning your remote working experience and working hours (GMT).
  3. 3Apply directly on the employer's careers page using the button below. Nomaders never handles your application.

Found 9h ago. Last checked 23 Sept. Always confirm the details on the original posting, salary and location can change after publication.

Listing sourced from Company boards.

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