Senior Clinical Project Manager Málaga

Puesto: Senior Clinical Project Manager Málaga)
Company Overview  Repro Novo is a Swiss clinical‑stage biopharmaceutical company committed to addressing critical gaps in male and female fertility as well as women's health. Our team is composed of proven experts with deep experience in reproductive medicine, drug development, regulatory affairs and business development who have successfully brought multiple therapies to market.
Job Overview  For our development site in Barcelona, Spain, we are looking for a Senior Clinical Project Manager. This office‑based role will work closely with cross‑functional international teams and external partners to oversee the execution of our clinical development programs. The position is based in Barcelona with flexibility for remote work, and requires approximately X% travel, including regular visits to Repro Novo’s development headquarters in Copenhagen and participation in relevant meetings and conferences.

Key Responsibilities   Plan, initiate and manage clinical trials, ensuring adherence to timelines, budgets and quality standards.
Develop and maintain project plans, including timelines and milestones.
Coordinate and communicate with cross‑functional teams, including Clinical Operations, Data Management, Regulatory Affairs and Biostatistics.
Monitor trial progress and implement corrective actions as necessary to ensure project objectives are met.
Ensure compliance with Good Clinical Practice (GCP), regulatory requirements and company SOPs.
Select, oversee and manage relationships with external vendors, including CROs, laboratories and other service providers.
Prepare and present project status reports to senior management and stakeholders.
Oversee the preparation of study‑related documents, including protocols, informed consent forms and case report forms.
Participate in the selection and training of clinical trial sites and investigators.
Ensure proper documentation and archiving of all trial‑related materials.
Identify, assess and manage risks associated with clinical trials, developing mitigation strategies to address potential issues.
Qualifications   Master’s or Bachelor’s degree in life sciences, nursing or another relevant life sciences field.
At least 5 years of clinical operations experience, including management of PhaseII and PhaseIII clinical trials.
Strong knowledge of clinical trial processes, regulations and guidelines, including ICH‑GCP.
Experience overseeing study timelines, risks and operational deliverables.
Fluency in English, both spoken and written.
Excellent organizational, communication and problem‑solving skills, with strong attention to detail.
Ability to manage multiple projects simultaneously and work effectively in a fast‑paced environment.
Proficiency in project management software and tools.
Benefits  At Repro Novo, you will join a focused, international team advancing clinical‑stage programs in areas of significant unmet medical need across fertility and women’s health. In this role, you will have the opportunity to:
Work in a high‑impact role as part of a passionate team of development experts.
Contribute to the advancement of clinical programs addressing critical therapeutic gaps in male and female infertility as well as women’s health.
Be part of a small, agile biotech organization where close collaboration across functions provides broad exposure to the full drug development process.
Gain visibility into key strategic and development decisions, working closely with senior leadership and experienced industry professionals.
We offer a collaborative, entrepreneurial environment where your contribution is visible, your expertise is valued, and your work supports clinical programs with clear purpose.

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