Senior Solutions Consultant

Warman O'Brien

Deutschland

Remote

EUR 90,000 - 130,000

Full time

27 hours ago
Be an early applicant
Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

Job summary

Warman O'Brien seeks a Senior Solutions Consultant to support its European expansion in life sciences software. You will combine consultative pre-sales, technical solution design and regulatory expertise to translate complex challenges into practical, compliant solutions.

You will guide customers from discovery through implementation handover, partnering with cross-functional teams. You will lead solution design, demonstrations and RFP responses while collaborating with product, engineering and

Qualifications

  • 7–12 years in solutions consulting or related roles in life sciences.
  • Experience supporting enterprise software in pharma or life sciences.
  • Familiarity with structured/regulated content management platforms.
  • Strong communication and stakeholder management skills.

Responsibilities

  • Partner with Account Executives to understand customer needs across regulatory, clinical, CMC, labeling, safety, quality and medical affairs.
  • Lead discovery sessions and translate customer challenges into tailored solutions and compelling business cases.
  • Deliver product demonstrations and technical walkthroughs to senior stakeholders; provide regulatory expertise throughout the sales process.
  • Collaborate with Product and Engineering to resolve technical barriers and inform roadmap priorities.

Skills

Solutions consulting
Sales engineering
Life sciences
Regulatory affairs

Education

Bachelor’s degree in Life Sciences or Computer Science

Tools

Veeva
OpenText
CARA

Job description

Location: Remote, Germany

Employment type: Permanent

Reporting to: Chief Revenue Officer

About the opportunity

We are partnering with an established life sciences software company to recruit a Senior Solutions Consultant to support its continued European expansion.

The company helps pharmaceutical and life sciences organisations create, manage and reuse regulated content through a structured content management platform.

Combining consultative pre-sales, technical solution design and life sciences expertise, you will help customers translate regulatory, scientific and operational challenges into practical solutions. You will support complex enterprise opportunities from initial discovery through to implementation handover, working closely with commercial, product and customer success teams.

This is a non-quota-carrying role, with responsibility for building customer confidence, demonstrating business value and ensuring proposed solutions meet technical and regulatory requirements.

Key responsibilities
Customer discovery and solution consulting
  • Partner with Account Executives to understand customer needs across regulatory, clinical, CMC, labelling, safety, quality and medical affairs.
  • Lead discovery sessions and translate customer challenges into tailored solutions and compelling business cases.
  • Deliver product demonstrations, technical walkthroughs and presentations to senior business and technical stakeholders.
  • Provide technical and regulatory expertise throughout the sales process, supporting discussions with IT, information security and procurement teams.
Solution design and technical readiness
  • Lead solution design discussions covering structured authoring, content reuse, metadata and enterprise integrations.
  • Configure platform environments and workflows for demonstrations, proof-of-concept activities and customer-specific use cases.
  • Develop proof-of-concept integrations and scripts where required.
  • Work with Customer Success to assess customer readiness, define initial implementation scope and ensure a smooth handover.
Cross-functional collaboration
  • Lead responses to RFPs and RFIs, contributing to security reviews and validation documentation.
  • Identify technical barriers and collaborate with Product and Engineering to resolve them.
  • Share customer insights to inform product development and roadmap priorities.
  • Represent the business in customer workshops, webinars, industry events and advisory discussions.
Experience and skills
  • Typically 7–12 years of relevant experience in solutions consulting, sales engineering, technical product management, implementation consulting or pharmaceutical digital transformation.
  • Experience supporting enterprise software customers within pharmaceutical or life sciences environments.
  • Familiarity with structured content management, regulatory information management or traditional content management platforms. Experience with Veeva, OpenText or CARA would be advantageous.
  • A track record of supporting complex opportunities involving global customers and multiple stakeholders.
  • Strong communication, storytelling and presentation skills, with the ability to explain technical concepts in terms of business and regulatory value.
  • Confidence leading both strategic customer conversations and detailed technical discussions.
  • Ability to manage multiple priorities and work effectively across commercial and technical teams.
Regulatory and technical knowledge
  • Strong understanding of relevant life sciences regulations and standards, including GxP, eCTD, IDMP and 21 CFR Part 11.
  • Knowledge of FHIR and its application to pharmaceutical content and data exchange, including ePI, ICH M11, M4Q(R2) and PQI/PQ-CMC.
  • Experience with metadata modelling, taxonomies, ontologies and controlled vocabularies to support structured content reuse.
  • Practical knowledge of REST APIs, JSON, XML and HTML, including configuring and troubleshooting integrations.
  • Understanding of information security and data privacy requirements, including ISO 27001, SOC 2, GDPR and HIPAA.
  • Familiarity with AI-enabled pharmaceutical workflows would be beneficial.
Qualifications
  • Bachelor’s degree in a relevant discipline, such as Computer Science, Life Sciences, Regulatory Affairs or Information Systems.
  • An advanced degree or relevant professional certification, such as RAC, PMP, TOGAF or AWS Solutions Architect, would be advantageous.
Personal attributes

You will thrive in this role if you are proactive, pragmatic and comfortable working in a small, evolving business. You should bring a collaborative, consultative approach, take ownership of outcomes and build customer credibility through expertise and clear communication.

The environment offers broad responsibility and opportunities to develop skills across commercial, technical and product functions.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Sr. Principal Consultant, Regulatory Strategy and Advisory
Sr. Principal Consultant, Regulatory Strategy and Advisory

Infosys Consulting • München

On-site
EUR 90,000 - 120,000
Lead Technical Solutions Scientist - Biopharma
Lead Technical Solutions Scientist - Biopharma

Roquette Laisa España SA • Germany

Hybrid
USD 79,908 - 102,739
Lead Customer Solutions Scientist (M/F) - Biopharma
Lead Customer Solutions Scientist (M/F) - Biopharma

Roquette Group • Germany

Remote
USD 79,908 - 102,739
Senior Implementation Consultant - Marketing & Medical Software (Remote)
Senior Implementation Consultant - Marketing & Medical Software (Remote)

Veeva Systems • Berlin

Remote
EUR 90,000 - 130,000
Senior Product Lifecycle Management Consultant - permanent role
Senior Product Lifecycle Management Consultant - permanent role

ProPharma • Germany

On-site
EUR 90,000 - 120,000
Lead Customer Solutions Scientist (M/F) - Biopharma
Lead Customer Solutions Scientist (M/F) - Biopharma

Roquette • Walsrode

On-site
EUR 70,000 - 90,000
Director, Business Development- Quality and Compliance
Director, Business Development- Quality and Compliance

ProPharma • Berlin

Hybrid
EUR 120,000 - 160,000
Regulatory Affairs Consultant – Germany & Austria (Munich on-site) m/f/d
Regulatory Affairs Consultant – Germany & Austria (Munich on-site) m/f/d

Parexel International • Germany

Hybrid
EUR 100,000 - 160,000
On-site Munich office
Regulatory Affairs Consultant – Germany & Austria (Munich on-site)
Regulatory Affairs Consultant – Germany & Austria (Munich on-site)

Parexel International • München

On-site
EUR 90,000 - 120,000
Senior Consultant: Life Sciences Digital Assets & PM Lead
Senior Consultant: Life Sciences Digital Assets & PM Lead

Veeva Systems • Germany

On-site
USD 102,762 - 171,271