Senior Clinical Operations Project Manager

Senior Clinical Operations Project Manager

Planet Pharma

Remote, Spain

Embark on a pivotal role within an innovative biotech powerhouse as a Senior Clinical Operations Project Manager, exclusively available through Planet Pharma. This position offers a unique chance to lead complex clinical trials directly with a Sponsor developing groundbreaking therapies and that has made cutting-edge R&D investments. Based remotely in Spain, you will be integral to a growing organization that thrives on agility, vision, and scientific excellence.

As a Senior CPM, you will oversee multiple clinical trials, ensuring seamless coordination between CROs, vendors, and internal teams. Your leadership will be critical in driving projects forward in a dynamic, sometimes unstructured environment that rewards proactive, solutions-oriented individuals. Join an expanding R&D landscape and contribute directly to pioneering treatments with global impact.

Required Skills and Qualifications:

• Minimum 7 years of experience as a Clinical Project Manager or Clinical Operations Project Manager within CRO or Biotech settings.
• Proven expertise in managing Phase I-III clinical studies, with a focus on Neuroscience, Ophthalmology, Immunology, and/or Rare Diseases.
• Strong background in vendor and budget management.
• Demonstrated ability to oversee clinical trial operations, ensuring compliance and quality standards.
• Excellent communication, leadership, and problem-solving skills, with a proactive and adaptable mindset suitable for a fast-paced environment.
• Experience managing multicenter international studies in Europe and the US.
• Familiarity with additional systems and processes relevant to clinical data management and regulatory compliance.
• Autonomy in navigating unorganized or evolving workflows with minimal supervision.
• Familiarity in eTMF systems such as Veeva Vault.

Preferred Education and Experience:

• Bachelor’s degree in Life Sciences, Pharmacy, or related field; Master’s degree or higher preferred.
• At least 7 years of direct experience in clinical trial management within CRO or biotech environments, with a proven track record of successful trial delivery.

Other Requirements:

• Candidates must be based in Spain and work remotely.
• Availability to participate in interviews with key stakeholders, including senior project directors and HR.
• Flexibility to support ongoing clinical studies within a growing, fast-evolving Sponsor.