Senior Consultant

Devote Consulting Group; Lisboa; Presencial; EUR 60 000 - 90 000; Tempo integral

Resumo da oferta

Devote Consulting is seeking a Senior Consultant to drive improvements in clinical operations, data, and GxP systems within Life Sciences R&D. You will lead projects, optimize business processes, and manage stakeholders to deliver compliant, data-driven solutions.

The role requires a master’s degree and 5+ years in regulated industries such as Pharma, Biotech, or MedTech, with English fluency and strong documentation skills.

Qualificações

• 5+ years of experience as a consultant or similar in regulated life sciences sectors.
• Experience creating compliance and validation documentation.
• Fluent in English with strong written and verbal communication.
• Experience with agile delivery methods and data-driven process optimization.
• Experience in Life Science R&D and regulatory affairs environments.

Responsabilidades

• Deliver changes in life sciences projects focusing on processes, data, and systems.
• Redesign and improve business workflows for greater efficiency.
• Lead planning, change management, and delivery of compliance documentation.
• Ensure project progress and maintain high-quality deliverables.

Conhecimentos

Stakeholder management

Analytical thinking

Change management

Regulated industry knowledge

English fluency

Formação académica

Master’s degree in business administration, IT, life sciences or equivalent

Ferramentas

CTMS

eTMF

EDC

QMS

RIMS

LIMS

Descrição da oferta de emprego

Join Our Team at Devote Consulting

SENIOR CONSULTANT CAREER OPPORTUNITY

Are you an experienced professional from the pharmaceutical industry, passionate about improving business processes and driving impactful change? Devote Consulting is expanding its team and is looking for a Senior Consultant with expertise in clinical operations, data, and GxP systems (e.g., CTMS, eTMF, EDC, QMS, RIMS, LIMS).

Are We Looking for You?

• You thrive in the fast-paced life of consulting and enjoy sharing your knowledge and ideas.
• You take ownership of your tasks, delivering high-quality work that makes a difference for patients.
• You have experience working with agile delivery methods and understand how to optimize business processes using data efficiently.
• You are excited about improving processes and implementing systems in Life Science R&D, including creating the required compliance documentation.
• You’ll excel in our high-achieving culture, with ample opportunities for both personal and professional growth.

What You’ll Do

As a Senior Consultant at Devote Consulting, your key responsibilities will include:

• Supporting projects: Deliver changes in the life sciences industry focused on processes, data, and systems within R&D, clinical operations, and regulatory affairs.
• Business process optimization: (Re)design and improve business workflows for greater efficiency.
• Stakeholder management: Lead project planning, change management, and delivery of compliance documentation.
• Driving project success: Ensure project progress and maintain high-quality standards for deliverables.

Your Qualifications

We’re looking for individuals with the following qualifications:

• A master’s degree in business administration, IT, life sciences or equivalent
• 5+ years of experience as a consultant, business analyst, project manager, or equivalent role in regulated industries such as Pharma, Biotech, or MedTech
• Proven analytical and problem-solving skills, with a passion for making an impact
• Experience in creating compliance and validation documentation
• Fluent in English, with excellent verbal and written communication skills
• Expertise in Clinical R&D systems (CTMS, eTMF, eSource, RBM, EDC, QMS, LIMS, etc.) and/or medical devices

What We Offer

At Devote Consulting, we offer a position where you can take responsibility, influence outcomes, and make a difference in your everyday work. You’ll lead one or more projects as a specialist, business analyst, or project manager, collaborating with clients to drive meaningful change in the pharmaceutical industry.