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.
Clinical Project Manager to oversee global oncology clinical trials within a CRO setting. The role involves managing project delivery, budgets, and cross-functional teams.
The Feasibility Manager delivers evidence-based assessments for clinical trials. The role offers the chance to work on complex oncology and rare disease programs.
This role manages global clinical research trials and portfolios, specifically within oncology. You will lead cross-functional teams, oversee study budgets, and ensure quality compliance.
This role manages regulatory submissions and site activation readiness for clinical trials. It offers the opportunity to work within a global clinical research organization.
Senior Medical Writer/Principal Medical Writer leading development of high-quality clinical study documents (protocols, IBs, DSURs, CSRs) for Precision Medicine Group, remote in Spain.
A Regulatory and Start Up Specialist is needed to manage clinical trial submissions and site activation in Spain.
Senior Clinical Research Associates will monitor clinical studies at investigative sites and ensure protocol compliance. The role offers a fully home-based arrangement within Spain.
Clinical Research Associate II will monitor clinical studies at investigative sites and ensure protocol compliance. The role offers a high-quality work-life balance and professional influence.
This role leads the governance and continuous improvement of Clinical Operations processes. It offers leadership opportunities in a global precision medicine organization.
The Site Contracts Manager will review, draft, and negotiate various legal agreements for clinical studies. This role offers full remote work options from Spain.
The Site Contracts Manager will review, draft, and negotiate various legal agreements for clinical studies. This role offers a fully remote working arrangement from Spain.
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.
Precision Medicine Group was founded in 1990 as a provider of clinical trial services and regulatory consulting. Over the years, it has expanded through strategic acquisitions to become a comprehensive life sciences partner, offering services from early-stage drug development to commercial launch. The company has grown significantly, establishing a global footprint with a strong focus on precision medicine and clinical trial excellence.