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Clinical Trial Manager

Remote from Spain·Added today (last checked 10 Nov)

Precision for Medicine

7 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
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
Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement

Nice to have

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

Education & certifications

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

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 for Medicine

Precision for Medicine is a global contract research organization (CRO) and clinical development services provider that supports the biopharmaceutical and life sciences industries. The company specializes in precision medicine, offering services that span from early-phase clinical trials to regulatory consulting, biomarker discovery, and patient recruitment. With a global footprint and a focus on accelerating the development of targeted therapies, Precision for Medicine operates across North America, Europe, and Asia, employing thousands of professionals in clinical operations, regulatory affairs, and related fields.

In Spain, Precision for Medicine has a growing presence, with clinical operations and project management roles based in the country. The company's Spanish team supports international clinical trials and collaborates with global colleagues, making it a relevant employer for international professionals with experience in clinical research, project management, and regulatory affairs. The work culture emphasizes scientific rigor, collaboration, and a patient-centric approach, offering opportunities for career growth in a dynamic, global environment.

Founded: 2012
Employees: 1,000–5,000
Headquarters: Bethesda, USA
In Spain: Madrid

Good to know if you are moving

Precision for Medicine is part of the Precision Medicine Group, which has a global presence with offices in the US, Europe, and Asia, offering opportunities for international mobility.
The company focuses on precision medicine and clinical trials, providing roles that are highly specialized and valuable for professionals with experience in clinical research and project management.
Spain-based roles, such as Clinical Project Manager and Clinical Research Associate, involve working on global trials, which can offer exposure to international regulatory environments and diverse patient populations.
The company's work culture emphasizes scientific innovation and collaboration, making it an attractive option for professionals looking to advance their careers in the clinical research industry.

In their own words

Additional information

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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All open roles at Precision for Medicine