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Clinical Trial Manager

Remote from Spain·Added 5 days ago (last checked 14 Nov)

Precision Medicine Group

4 open roles

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Our summary

Work mode: Remote from Spain
English: Required
Education: University degree

Visa options

The ad rules out sponsorship
Per the ad: “Candidates must be legally authorized to work in the country of employment without employer sponsorship.”

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Skills

Requirements

What we're looking for

You love having responsibility and a say in how clinical trials are run
You plan ahead, but have alternative options and a flexible approach
You are client focused
You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.
You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly
You are a master at identifying any risks that threaten projects and handle them resolutely
You thrive and work with autonomy and ownership to deliver successful outcomes

Minimum Required:

Bachelor's degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology

Other Required:

Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated 'clinical lead' role).
Significant clinical trial management experience in the area of oncology
Working knowledge of GCP/ICH guidelines and the clinical development process
Availability for domestic and international travel including overnight stays
Must be able to communicate effectively in the English language
Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)
Demonstrated ability to develop positive working relationships with internal and external organizations
Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan

Nice to have

Experience with CAR-T and Radiopharmaceuticals would be a strong plus

Pay & benefits

Visa & relocation

Candidates must be legally authorized to work in the country of employment without employer sponsorship.

The role

Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team. Candidates can work remotely in Hungary, Poland, Romania, Serbia, Slovakia, UK or Spain.

Precision for Medicine is a precision medicine CRO. 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, in addition to working across other therapeutic areas.

You will be the hub of central intelligence for the studies you will be managing and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity.

We are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don't miss exploring working with us.

What you'll do

The day-to-day role, and how we will support your continued growth:

Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out
Successful execution of assigned trials and ensuring completion of trial deliverables
Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members
Mentoring and training of team members
Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor
Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities
Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction

About Precision Medicine Group

Precision Medicine Group is a global life sciences company that provides a comprehensive suite of services and solutions to the pharmaceutical, biotech, and medical device industries. The company operates across the entire drug development lifecycle, from clinical trial design and regulatory consulting to laboratory services, data management, and commercial distribution. With a workforce of several thousand employees worldwide, Precision Medicine Group supports its clients through a network of offices across North America and Europe, helping to bring new therapies to market efficiently and effectively.

In Spain, Precision Medicine Group has established a presence to support the growing clinical trial and research activities in the region. The company's Spanish operations focus on providing clinical trial management, feasibility, and site contract services, which are critical for international professionals looking to enter the Spanish life sciences job market. The work culture emphasizes scientific rigor, regulatory compliance, and a collaborative environment, making it a relevant employer for those with backgrounds in clinical research, life sciences, or regulatory affairs.

Founded: 1990
Employees: 5,000–10,000
Headquarters: Bethesda, USA
In Spain: Barcelona

Good to know if you are moving

The company has a global presence with offices in North America and Europe, offering opportunities for international professionals.
Spain is a key market for the company's clinical trial services, with roles focused on feasibility, site contracts, and project management.
The company values regulatory and clinical expertise, making it a good fit for professionals with backgrounds in life sciences, nursing, or regulatory affairs.
The work environment is collaborative and project-based, with a focus on quality and compliance.
Fluency in English is essential, and knowledge of Spanish is a plus for working with local sites and authorities.

In their own words

Additional information

Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement

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.

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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 myHR@precisionmedicinegrp.com.

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