Senior Consultant

Devote Consulting Group; København; On-site; DKK 850,000 - 1,100,000; Full time

Job summary

Devote Consulting is seeking a Senior Consultant with extensive experience in clinical operations, data and GxP systems to drive change for pharmaceutical clients in Denmark. You will lead projects, analyze processes, and implement systems across R&D, clinical operations, and regulatory affairs.

You’ll collaborate with stakeholders, design compliant documentation, and deliver high-quality results in a fast-paced consulting environment that values growth and knowledge sharing.

Qualifications

• Master's degree in business administration, IT or life sciences.
• 5+ years of experience as a consultant in regulated industries such as Pharma, Biotech, or MedTech.
• Proven analytical and problem-solving skills with a passion for impact.
• Experience creating compliance and validation documentation.
• Fluent in English with excellent communication skills.
• Expertise in Clinical R&D systems (CTMS, eTMF, EDC, QMS, LIMS) and/or medical devices.

Responsibilities

• Support projects in life sciences focusing on processes, data, and systems in R&D, clinical operations, and regulatory affairs.
• Redesign and improve business workflows for efficiency.
• Lead project planning, change management, and delivery of compliance documentation.
• Drive project success and ensure high-quality deliverables.

Skills

Agile delivery

Stakeholder management

Analytical thinking

Communication in English

Education

Master's degree in business administration / IT / life sciences

Tools

CTMS

eTMF

EDC

QMS

LIMS

Job description

Join Our Team at Devote Consulting

SENIOR CONSULTANT CAREER OPPORTUNITY

Join Our Team at Devote Consulting

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.

Ready to Join Us?

We welcome individuals from all backgrounds and are committed to a recruitment process that ensures equal opportunities for all applicants.

We review applications on a rolling basis.