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Key Responsibilities:
- Manage site activation and regulatory submissions for clinical trials in Spain.
- Oversee contract and budget negotiations with sites to ensure timely approvals.
- Collaborate with cross-functional teams to maintain project documentation and timelines.
Qualifications:
- Bachelor's degree in life sciences or related field; regulatory and startup experience in CRO or pharma.
- Proven experience in contracts and budgeting negotiation within clinical research.
- Fluency in English and Spanish; Portuguese is a plus.
Additional Requirements:
- Strong communication and organizational skills for managing multiple priorities.
- Familiarity with electronic information systems and milestone tracking tools.
- Knowledge of local clinical trial laws and ICH-GCP principles.
Precision for Medicine
Precision for Medicine is a global Clinical Research Organization specializing in precision medicine for rare diseases and oncology. The company is experiencing continued growth and values operational excellence and regulatory expertise.