Senior Consultant

Devote Consulting

København

Hybrid

DKK 900,000 - 1,300,000

Full time

14 days+
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Job summary

Devote Consulting wants a Senior Consultant to drive improvements in clinical operations, data management, and GxP systems across R&D, regulatory affairs, and operations.

You will design processes, manage stakeholders, and deliver compliant documentation while guiding projects with agile practices in a fast-paced consulting environment.

Qualifications

  • Master's degree in business administration, IT, life sciences or equivalent.
  • 5+ years of experience as a consultant in regulated industries such as Pharma, Biotech, or MedTech.
  • Analytical and problem-solving skills with the ability to drive impact.
  • Experience creating compliance and validation documentation.
  • Fluent in English with strong written and verbal communication.

Responsibilities

  • Support projects delivering changes in life sciences focusing on processes, data, and systems in R&D, clinical operations, and regulatory affairs.
  • Design and improve business workflows for greater efficiency.
  • Lead project planning, change management, and delivery of compliance documentation.
  • Ensure project progress and maintain high-quality deliverables.

Skills

Analytical skills
Problem solving
English fluency
Stakeholder management

Education

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

Tools

CTMS
eTMF
EDC
QMS
LIMS

Job description

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.

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