
LINK Medical Research AB · Stockholm
LINK Medical is searching for a highly motivated Principal Consultant Clinical Pharmacology & DMPK in Sweden (Stockholm, Uppsala or Lund), Denmark (Copenhagen) ...
LINK Medical is searching for a highly motivated Principal Consultant Clinical Pharmacology & DMPK in Sweden (Stockholm, Uppsala
or Lund), Denmark (Copenhagen) and Norway (Oslo).
In this role, you will work in close collaboration with our local and international clients, being responsible for leading and
managing Clinical Pharmacology and DMPK activities throughout the drug development lifecycle—ensuring scientific excellence,
regulatory compliance, and efficient project delivery.
Responsibilities
of drug development programs.
Desired qualifications
(popPK).
Personal Characteristics
LINK Medical offers
We offer an exciting and challenging position in a European CRO that has a strong local presence. The company focuses on
collaboration, sharing of experience and continuous development of our employees in an international environment and values as
honest and open communication are essential. You will be given meaningful tasks requiring efficient collaboration between
industry, clinical and scientific teams, and the authorities. Besides a great working environment with dedicated and supporting
colleagues, we also offer a competitive compensation, benefit scheme and great development opportunities for all employees.
Contact Information
If you would like to know more or if you have any questions about the position, please contact:
Ulrika Andersson, Senior Director Drug Development,
+46 76 492 4518, Ulrika.andersson@linkmedical.eu
All applications are treated confidentially and will be evaluated when received, so please apply as soon as possible. Please
submit your application in English.
Last day for application: 31st of August, 2026.
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds... ClinChoice is searching for a Clinical R Programmer/ Principal Data Scientist Consultant to join one of our clients. We are seeking a Principal Data Scientist with strong experience in R and a solid background in clinical programming. The ideal candidate will have hands-on experience developing SDTM and ADAM datasets using R, along with working knowledge of SAS. This role requires someone who can support clinical trial deliverables, ensure regulatory compliance, and collaborate closely with biostatistics and clinical data teams. KEY RESPONSIBILITIES * Develop, validate, and maintain SDTM and ADaM datasets using R following CDISC standards. * Support TLF (Tables, Listings, Figures) generation in R or SAS as needed. * Write efficient, reproducible, and well-structured R scripts for clinical data analysis and reporting. * Collaborate with statisticians, data managers, and clinical teams to understand programming requirements. * Perform QC checks, reconcile data issues, and ensure deliverables meet regulatory expectations (e.g., FDA, EMA). * Contribute to programming workflows, documentation, and version control best practices. * Support automation initiatives and R-based pipeline development. * Utilize SAS for legacy studies or where SAS support is required. REQUIRED QUALIFICATIONS * Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field. * 4–6+ years of experience in clinical programming, with a strong focus on R. * Proven experience in creating SDTM and ADaM datasets using R. * Working knowledge of SAS programming. * Solid understanding of CDISC standards (SDTM, ADaM). * Experience with clinical trial data, regulatory submissions, and QC processes. * Strong analytical, problem-solving, and documentation skills. PREFERRED QUALIFICATIONS * Experience with R packages such as tidyverse, haven, pharmaverse (e.g., admiral, tidyCDISC), or other clinical programming toolkits. * Understanding of R Markdown, Shiny apps, or reproducible reporting tools. * Exposure to GxP validation, version control (Git), and automated workflows. * Experience working in a CRO or pharmaceutical environment. The Application Process Once you have submitted your CV, you will receive an acknowledgement that we have received it. If you have the requirements we need, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset, and they are the fulcrum around which all ClinChoice activities are built, and close management and training are the core instruments to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our low industry-average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent, guided by a commitment to diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. #LI-TT1 #LI-Remote #LI-Principal #Contract
PURPOSE: This role is ideal for an experienced Project Manager – Healthcare Technology with a strong background in construction-based project delivery, ideally gained within healthcare, infrastructure or other complex regulated environments. The successful candidate will have experience managing projects delivered through Principal Contractors under NEC-style contracts and be comfortable coordinating multiple stakeholders across live operational sites. Experience delivering technology or integrated systems within healthcare would be highly advantageous. KEY RESPONSIBILITIES: * Manage customer delivery projects of medium to large size, working within agreed contract scope, assumptions, constraints, budgets and timelines * Plan and manage projects end to end, applying appropriate project management standards, tools, governance and reporting disciplines * Coordinate installation, integration, commissioning, testing, acceptance and handover activities, ensuring all work is delivered to the required quality and safety standards * Manage project risks, dependencies, milestones, decision points and resource plans, taking proactive action to keep delivery on track * Protect project margins by monitoring cost elements, including labour, subcontractor activity, hardware and materials, and escalating deviations promptly * Act as the main interface with customers, subcontractors, suppliers and internal teams, ensuring clear communication and effective stakeholder management throughout the project lifecycle * Create and maintain project documentation, including status reports, risk logs, change records and handover documentation for Customer Care or support teams * Deliver projects in accordance with NEC4 or equivalent construction contract frameworks, ensuring contractual obligations, programme milestones and change control are effectively managed * Work closely with Principal Contractors, M&E contractors, consultants, subcontractors and client representatives to coordinate delivery activities throughout the construction programme * Manage delivery within live hospital environments, ensuring minimal disruption to clinical services whilst maintaining compliance with infection control, permit-to-work and site safety requirements * Lead project change management including Early Warning Notices (EWNs), compensation events, variations and scope changes where applicable * Coordinate technical design reviews, site surveys, construction readiness, commissioning activities, witness testing, customer acceptance and final handover * Ensure compliance with CDM regulations, RAMS, permit processes and site-specific health and safety requirements * Manage multiple concurrent projects across various locations, balancing customer priorities, internal resources and commercial objectives Experience and qualifications: * Project Management qualification or certification, such as PRINCE2, PMP, APM or equivalent, would be beneficial * Proven experience managing construction-related projects, ideally involving infrastructure, cabling, technology deployment or site-based delivery * Strong project management capability, with experience planning, monitoring and delivering projects against agreed milestones, budgets and quality standards * Experience managing project risks, dependencies, change control, resource planning and stakeholder expectations * Experience working under NEC3/NEC4 or similar construction contract frameworks * Experience delivering projects within live healthcare environments would be highly desirable * Experience delivering technology, communications, nurse call, security, fire, AV, BMS or other integrated building systems would be advantageous Skills and competencies: * Excellent project management, planning, organisation and delivery skills * Strong stakeholder management and communication skills, with the confidence to work with customers, subcontractors, suppliers and internal teams * Ability to manage multiple workstreams and competing priorities in complex or sensitive operational environments * Strong commercial awareness, including cost control, margin protection and contract-based delivery * Reporting skills and attention to detail * Basic experience in contractual law applicable for customer delivery projects * Build strong relationships across clinical, estates, IT and construction stakeholders, ensuring all parties remain aligned throughout project delivery * Excellent planning skills with the ability to manage complex construction programmes, critical paths and interdependencies * Strong understanding of construction site processes, commissioning activities and phased handovers * Ability to confidently challenge programme issues, negotiate solutions and influence stakeholders at all levels * Experience managing subcontractor performance and coordinating multidisciplinary delivery teams * Comfortable working independently whilst managing multiple concurrent projects across geographically dispersed sites * CSCS card or equivalent site qualification would be advantageous and SMSTS or SSSTS would be desirable.
CHANCE Als Teil der Clarius Group gehören wir zu den führenden Managed Service Providern in Deutschland. Unser Ziel: Prozesse intelligenter gestalten, Komplexität reduzieren und unseren Kunden den Freiraum geben, sich auf ihr Kerngeschäft zu konzentrieren. Daten, GenAI und Automatisierung entfalten ihren Wert nur dann, wenn sie fachlich richtig eingeordnet, analytisch durchdrungen und nachhaltig in Geschäftsprozesse integriert werden. In dieser Rolle arbeitest du bei Clarius Group in der Rolle des Trusted Advisors für unsere Kunden. Du berätst Fachbereiche und Management auf Augenhöhe, strukturierst komplexe Fragestellungen und verantwortest die inhaltliche und organisatorische Steuerung mehrerer Themenbereiche. Zur Verstärkung unseres Teams suchen wir genau Dich: Principal Consultant – Data, AI & Process Transformation (w/m/d) * Festanstellung * unbefristet * Vollzeit * ab sofort * Standort: Eschborn (Möglichkeit zum mobilen Arbeiten) AUFGABEN * Beratung von Fachbereichen und Management als Trusted Advisor zu Data-, Analytics-, GenAI- und Automatisierungsthemen * Analyse und Verständnis von Geschäftsprozessen, Entscheidungslogiken und fachlichen Zielsetzungen * Strukturierung komplexer fachlicher, analytischer und organisatorischer Fragestellungen * Übersetzung von Business-Zielen in analytische Fragestellungen, Zielbilder und priorisierte Initiativen * Gemeinsame Entwicklung von Zielbildern, Roadmaps und Prioritäten mit den Kunden * Einordnung fachlicher Anforderungen vor dem Hintergrund technischer Möglichkeiten und Grenzen * Aufbau wiederverwendbarer Vorgehensmodelle, Entscheidungsgrundlagen und Standards * Mitwirkung am Aufbau und an der Weiterentwicklung skalierbarer Beratungs- und Delivery-Strukturen PROFIL * Mehrjährige Erfahrung in einer beratenden Rolle im Umfeld von Data, BI, Analytics, AI oder Prozessautomatisierung * Nachweisbare Erfahrung als Sparringspartner für Fachbereiche und Management * Ausgeprägte Fähigkeiten im Bereich Business Analytics: * Verständnis von Geschäftsprozessen und KPIs * Ableitung analytischer Fragestellungen aus Business-Zielen * Bewertung von Daten, Analysen und Ergebnissen im fachlichen Kontext * Sehr gutes technisches Verständnis von: * BI- und Datenarchitekturen (z. B. Power BI, DWH, Lakehouse) * analytischen Modellen und Entscheidungslogiken * produktiven GenAI-Anwendungen * Automatisierung von Geschäftsprozessen * Fähigkeit, komplexe fachliche und technische Zusammenhänge verständlich zu vermitteln * Erfahrung in der Führung interdisziplinärer Teams (fachlich und disziplinarisch) * Sehr gute Kommunikations- und Moderationsfähigkeit * Strukturierte, eigenständige und verantwortungsbewusste Arbeitsweise * Sehr gute Deutschkenntnisse sowie gute Englischkenntnisse Wichtig zu wissen ist, dass es sich bei der Rolle nicht um eine operative Entwicklungs- oder Implementierungsposition handelt. Der Fokus liegt stattdessen auf Beratung, Analyse, Strukturierung und Entscheidungsfindung. Technische Tiefe dient dabei vor allem als Grundlage für Glaubwürdigkeit, nicht als Tagesgeschäft. Die Tätigkeit ist projektbezogen, mit hoher Kundennähe, und zeichnet sich durch eine Rolle mit hoher Sichtbarkeit und Verantwortung aus. WARUM WIR? Du führst komplexe Themen genau dort, wo Entscheidungen getroffen werden, und arbeitest an abwechslungsreichen Projekten bei anspruchsvollen Kunden. In deiner Rolle als Trusted Advisor hast du echten Einfluss und verbindest Business-Verständnis, Analytics, Technologie und Führung. Dabei erhältst du hohen Gestaltungsspielraum, übernimmst klare Verantwortung und arbeitest in einer wertschätzenden Kultur mit kurzen Entscheidungswegen. Gleichzeitig bietet dir die Position eine langfristige Perspektive, um aktiv am Aufbau eines skalierbaren Consulting- und Delivery-Bereichs mitzuwirken. Das ist Clarius. * Wachsendes Unternehmen mit Start-up-Spirit und echter Gestaltungsfreiheit * Hybrides Arbeiten: Büro in Eschborn + Möglichkeit zum mobilen Arbeiten * Abwechslungsreiche Aufgaben in einem dynamischen Arbeitsumfeld, das sich stetig weiterentwickelt * Weiterbildungs- und Entwicklungsmöglichkeiten * Attraktives Gehaltspaket inkl. Zusatzleistungen (z. B. JobRad, Geburtstagskuchen, etc.) Bring Deine Stärken ein, wo sie wirklich zählen und gestalte Deine Zukunft mit uns – bei der Clarius Group. Neue Ideen und Impulse sind bei uns nicht nur willkommen, sondern ausdrücklich gefragt: Echte Veränderung entsteht nur gemeinsam – mit Menschen, die mitdenken, mitgestalten und mit uns wachsen wollen. Und was Dich bei uns erwartet, ist mehr als nur ein Job: Freu Dich auf eine offene, herzliche Teamkultur, in der gegenseitige Unterstützung zählt - und ein großartiges, wertschätzendes Team, das Zusammenhalt wirklich lebt. Und weil Arbeiten auch Spaß machen darf, gehören Team-Events und gemeinsame Mitarbeiteraktionen bei uns ganz selbstverständlich dazu. Bewirb Dich mit deinen vollständigen Unterlagen inkl. Gehaltsvorstellung & frühestmöglichem Eintrittstermin - ganz einfach per E-Mail oder Online-Formular.