Senior Project Management Coordinator

Chemo; Cádiz; Presencial; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company is seeking a motivated Project Manager to oversee drug development projects, coordinating cross-functional teams and managing project budgets. The ideal candidate is fluent in Spanish and English, possesses project management skills, and may hold a PMP certification. This role offers a flexible working schedule and a permanent contract with added benefits.

Servicios

Flexible start times

Co-payment in voluntary health insurance

Formación

• Fluency in Spanish and English; knowledge of additional languages is a plus.
• PMP certification is advantageous.
• Experience in managing drug development projects.

Responsabilidades

• Manage and execute projects related to the development and commercialization of generic drugs.
• Coordinate cross-functional teams to ensure project objectives are met.
• Monitor project progress, risks, and issues.

Conocimientos

Fluency in Spanish

Fluency in English

Project Management

Coordination

Communication

Educación

PMP certification

Descripción del empleo

INSUD PHARMA Project Manager Job Description

INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health.

We are seeking a motivated and client-oriented Project Manager to join our growing team. The candidate will manage moderately large or complex projects related to drug development, primarily focusing on generic pharmaceuticals. Responsibilities include :

• Assisting in managing and executing projects related to the development and commercialization of generic drugs.
• Understanding the needs of internal and external customers and aligning projects with strategic guidelines.
• Coordinating cross-functional teams (R&D, regulatory affairs, clinical, manufacturing, patents, sales) to ensure project objectives are met.
• Analyzing project characteristics and processes end-to-end.
• Supporting the creation and maintenance of project schedules, timelines, budgets, and documentation.
• Preparing reports and updates for senior management and stakeholders.
• Monitoring project progress, risks, issues, and delays, and implementing mitigation plans.
• Managing project budgets and deviations.
• Developing systems and communication processes (CRM, BI, etc.) for project control.
• Revising project plans, status, and budgets for short- and mid-term planning.
• Reporting deviations and revising sales expectations, NPV, and business cases regularly.

Qualifications include fluency in Spanish and English; knowledge of additional languages is a plus. PMP certification is advantageous. The role offers flexible start times (Monday to Friday, full-time 40 hours) and a permanent contract. Benefits include co-payment in voluntary health insurance.

The interview process may be in-person or virtual, involving one or two interviews and possibly a test. We promote equal opportunities and do not discriminate based on ethnicity, religion, age, sex, nationality, marital status, sexual orientation, gender identity, disability, or other personal circumstances. Follow us on social media for updates.

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