{"data":{"id":158319,"slug":"chief-medical-officer-till-klinisk-forskningsverksamhet","type":"job","title":"Chief Medical Officer for Clinical Research Operations","description":"Do you want to be part of driving the development of tomorrow's medicines and medical technology products? At CTC, you have the opportunity to combine clinical research with medical leadership in a senior role where you contribute to both medical decisions and the long-term development of our operations.\n\nCTC was founded in 2011 and is a full-service CRO (Clinical Research Organisation) with six research clinics across Sweden, three of which are in Uppsala. One of these is a First-in-Human unit located at Uppsala University Hospital where new drugs are tested for the first time in humans. We conduct clinical trials in all therapeutic areas throughout the development process \u2013 from early to late phase. At CTC, approximately ten physicians with different backgrounds and specialties work as both permanent and consulting employees. By conducting clinical trials with high quality and a strong patient focus, CTC contributes to tomorrow's healthcare.\n\nWe are now seeking a board-certified specialist physician who wants to combine the role of senior research physician with overall medical responsibility for CTC's operations and development.\n\nAbout the Position\n\nAs Chief Medical Officer (CMO) at CTC, you have a central role in our clinical operations as well as in company management. You combine active clinical work as a principal investigator in drug studies in accordance with applicable regulations and quality standards with overall medical management and patient safety responsibility for CTC's clinics. You also represent CTC in various external contexts and interact and build relationships with customers, authorities, and hospital management.\n\nThe role also includes leading, supporting, and developing CTC's physician group, as well as holding personnel and budget responsibility for the physician group. Working toward close collaboration between the physician group and all of CTC's departments and business areas is central to the role in order to ensure high medical quality, good leadership, optimal medical staffing, and continued development of operations. The role reports to CTC's CEO.\n\nKey Responsibilities\n\nYour responsibilities include:\n\n- Act as principal investigator and sub-investigator in clinical studies conducted at CTC's clinics.\n- Ensure that medical processes and procedures at CTC guarantee research participants' safety, comply with relevant and current laws and regulations, national and international guidelines as well as quality standards, and are appropriate and effective for the organization.\n- Conduct medical risk assessments of studies planned at CTC's clinics and ensure the feasibility of studies for CTC.\n- Oversee and follow up on CTC's patient safety work, including leading investigations of suspected adverse events and reporting serious adverse events to relevant authorities in accordance with applicable laws and regulations.\n- Represent CTC in contact with external parties such as authorities, hospital management, professional organizations, patient organizations, key opinion leaders, and the public to strengthen CTC's position within the local and national life sciences community.\n- Represent CTC in customer meetings to establish new customer relationships, provide medical expertise, and support study teams within CTC.\n- Lead and develop CTC's scientific profile in collaboration with the internal organization, customers, and academic partners.\n- Lead and develop the physician group's medical work.\n- Participate in relevant management groups within CTC and advise CTC's CEO on medical matters.\n\nAbout You\n\nYou work independently and proactively, with the ability to make well-founded decisions and drive matters forward. You quickly grasp new issues and therapeutic areas and understand and take into account different stakeholders' perspectives. You are structured and solution-oriented and thrive in a role where you contribute to continuous development of operations. You are a confident and approachable leader with the ability to motivate and develop both employees and operations. You easily build good and trusting relationships and collaborate successfully with different professions and stakeholders. We place great emphasis on personal suitability.\n\nRequirements\n\n- Swedish medical license with specialist competence in an area relevant to the position\n- PhD in Medical Science\n- Solid experience in clinical research, clinical trials, and GCP\n- Excellent ability to communicate in Swedish and English, both orally and in writing\n\nMeritorious\n\n- Experience in management positions, medical management responsibility, operational development, and\/or systematic patient safety work\n- Experience working in the life sciences industry, at pharmaceutical companies, or in authorities with responsibility for pharmaceutical matters\n\nWhat We Offer\n\nWith us, you become part of a knowledge-intensive organization where research, medical quality, and innovation are in focus. You have the opportunity to influence both operational development and future drug treatments while holding overall medical responsibility. We offer a stimulating work environment with short decision-making paths, close collaboration, and an open climate where experiences and knowledge are shared among colleagues. We view positively your desire to maintain clinical engagement within your medical specialty or within research, and are therefore open to discussing the scope of the position.\n\nAs an employee, you are covered by a collective agreement, and we value balance between work and personal life through, among other things, flexible working hours, wellness allowance, and generous vacation benefits.\n\nSounds exciting or do you have questions?\n\nContact CEO Suzanne Iverson Hemberg, suzanne.iverson.hemberg@ctc-ab.se\n\nApplication deadline: September 14, 2026. Start date by agreement.\n\nAbout the Employer \u2013 CTC Clinical Trial Consultants AB\n\nCTC Clinical Trial Consultants AB is a Clinical Research Organisation (CRO) with operations in Uppsala, Stockholm, Link\u00f6ping, and Gothenburg.\n\nAs a CRO, we conduct clinical studies on behalf of industry and academia and offer a complete full-service package of the services, activities, and deliverables required to conduct a clinical trial. We currently conduct studies from early to late phase (phases 0-IV).\n\nStudies are conducted primarily at our own clinics but also in collaboration with external clinics.\n\nApproximately 125 employees work with us, about half of whom work clinically. The headquarters is located in Uppsala.","language":"sv","is_translated":true,"title_original":"Chief Medical Officer till klinisk forskningsverksamhet","description_original":"Vill du vara med och driva utvecklingen av framtidens l\u00e4kemedel och medicintekniska produkter? Hos CTC f\u00e5r du m\u00f6jlighet att kombinera klinisk forskning med medicinskt ledarskap i en senior roll d\u00e4r du bidrar till b\u00e5de medicinska beslut och den l\u00e5ngsiktiga utvecklingen av v\u00e5r verksamhet. \nCTC grundades 2011 och \u00e4r ett full-service CRO (Clinical Research Organisation) med sex egna forskningskliniker runt om i Sverige, varav tre i Uppsala. En av dessa \u00e4r en First-in-Human-enhet placerad p\u00e5 Akademiska sjukhuset d\u00e4r nya l\u00e4kemedel pr\u00f6vas f\u00f6r f\u00f6rsta g\u00e5ngen i m\u00e4nniska. Vi bedriver kliniska pr\u00f6vningar inom samtliga terapeutiska omr\u00e5den och genom hela utvecklingen \u2013 fr\u00e5n tidig till sen fas. P\u00e5 CTC arbetar ett tiotal l\u00e4kare med olika bakgrund och specialiteter, b\u00e5de som tillsvidareanst\u00e4llda och konsultanst\u00e4llda. Genom att genomf\u00f6ra kliniska pr\u00f6vningar med h\u00f6g kvalitet och ett starkt patientfokus bidrar CTC till morgondagens h\u00e4lso- och sjukv\u00e5rd. \nNu s\u00f6ker vi en disputerad specialistl\u00e4kare som vill kombinera rollen som senior forskningsl\u00e4kare med ett \u00f6vergripande medicinskt ansvar f\u00f6r CTC:s verksamhet och utveckling. \nOm tj\u00e4nsten \nSom Chief Medical Officer (CMO) hos CTC har du en central roll i v\u00e5r kliniska verksamhet s\u00e5v\u00e4l som i f\u00f6retagets ledning. Du kombinerar ett aktivt kliniskt arbete som huvudpr\u00f6vare i l\u00e4kemedelsstudier i enlighet med g\u00e4llande regelverk och kvalitetsstandard med ett \u00f6vergripande medicinskt lednings- och patients\u00e4kerhetsansvar f\u00f6r CTC:s kliniker. Du representerar ocks\u00e5 CTC i olika externa sammanhang och interagerar samt bygger relationer med b\u00e5de kunder, myndigheter och sjukhusledningar. \nI rollen ing\u00e5r ocks\u00e5 att leda, st\u00f6tta och utveckla CTC:s l\u00e4kargrupp, samt att inneha personal- och budgetansvar f\u00f6r l\u00e4kargruppen. Att verka f\u00f6r ett n\u00e4ra samarbete mellan l\u00e4kargruppen och CTC:s samtliga avdelningar och aff\u00e4rsomr\u00e5den \u00e4r centralt f\u00f6r rollen i syfte att s\u00e4kerst\u00e4lla h\u00f6g medicinsk kvalitet, ett gott ledarskap, optimal medicinsk bemanning och en fortsatt utveckling av verksamheten. Rollen rapporterar till CTC:s VD. \nArbetsuppgifter \nI rollen ing\u00e5r bland annat att: \n- Agera huvudpr\u00f6vare och medpr\u00f6vare i kliniska studier som genomf\u00f6rs p\u00e5 CTC:s kliniker. \n- Ansvara f\u00f6r att medicinska processer och rutiner p\u00e5 CTC garanterar forskningsdeltagarnas s\u00e4kerhet, f\u00f6ljer relevanta och aktuella lagar och f\u00f6rordningar, nationella och internationella riktlinjer samt kvalitetsstandarder och \u00e4r \u00e4ndam\u00e5lsenliga och v\u00e4lfungerande f\u00f6r organisationen. \n- Genomf\u00f6ra medicinska riskbed\u00f6mningar av studier som planeras p\u00e5 CTC:s kliniker och s\u00e4kerst\u00e4lla studiernas genomf\u00f6rbarhet f\u00f6r CTC. \n- Ansvara f\u00f6r och f\u00f6lja upp CTC:s patients\u00e4kerhetsarbete, inklusive leda utredningar av fall av misst\u00e4nkt v\u00e5rdskada samt rapportera allvarliga v\u00e5rdskador till relevanta myndigheter i enlighet med g\u00e4llande lagar och regelverk. \n- Representera CTC i kontakt med externa parter s\u00e5som myndigheter, sjukhusledningar, professionella organisationer, patientorganisationer, key opinion leaders och allm\u00e4nheten f\u00f6r att st\u00e4rka CTC:s position inom det lokala och nationella life-science samh\u00e4llet. \n- Representera CTC i kundm\u00f6ten i syfte att etablera nya kundrelationer, tillhandah\u00e5lla medicinsk expertis och st\u00f6tta studieteam inom CTC.  \n- Leda och utveckla CTC:s vetenskapliga profil i samarbete med den interna organisationen, kunder och akademiska partners. \n- Leda och utveckla l\u00e4kargruppens medicinska arbete. \n- Delta i relevanta ledningsgrupper inom CTC samt r\u00e5dge CTC:s VD i medicinska fr\u00e5gor. \nVi s\u00f6ker dig som arbetar sj\u00e4lvst\u00e4ndigt och proaktivt, med f\u00f6rm\u00e5ga att fatta v\u00e4lgrundade beslut och driva fr\u00e5gor fram\u00e5t. Du har l\u00e4tt f\u00f6r att snabbt s\u00e4tta dig in i nya fr\u00e5gest\u00e4llningar och terapiomr\u00e5den samt f\u00f6rst\u00e5r och tillgodoser olika intressenters perspektiv. Du \u00e4r strukturerad och l\u00f6sningsorienterad och trivs i en roll d\u00e4r du bidrar till kontinuerlig utveckling av verksamheten. Du \u00e4r en trygg och prestigel\u00f6s ledare med f\u00f6rm\u00e5ga att motivera och utveckla b\u00e5de medarbetare och verksamhet. Du har l\u00e4tt f\u00f6r att skapa goda och f\u00f6rtroendefulla relationer och samarbetar framg\u00e5ngsrikt med olika professioner och intressenter. Vi l\u00e4gger stor vikt vid personlig l\u00e4mplighet. \nKrav\n- Svensk l\u00e4karlegitimation med specialistkompetens inom ett f\u00f6r tj\u00e4nsten relevant omr\u00e5de \n- Disputerad (PhD) inom medicinsk vetenskap \n- Gedigen erfarenhet av klinisk forskning, kliniska pr\u00f6vningar och GCP \n- Mycket god f\u00f6rm\u00e5ga att kommunicera p\u00e5 svenska och engelska i s\u00e5v\u00e4l tal som skrift\nMeriterande\n- Erfarenhet av chefsuppdrag, medicinskt ledningsansvar, verksamhetsutveckling och\/eller systematiskt patients\u00e4kerhetsarbete \n- Erfarenhet av arbete inom life-science industrin, p\u00e5 l\u00e4kemedelsbolag eller myndighet med ansvar f\u00f6r l\u00e4kemedelsfr\u00e5gor \n\n\nVi erbjuder \nHos oss blir du en del av en kunskapsintensiv organisation d\u00e4r forskning, medicinsk kvalitet och innovation st\u00e5r i fokus. Du f\u00e5r m\u00f6jlighet att p\u00e5verka b\u00e5de verksamhetens utveckling och framtidens l\u00e4kemedelsbehandlingar samtidigt som du har ett \u00f6vergripande medicinskt ansvar. Vi erbjuder en stimulerande arbetsmilj\u00f6 med korta beslutsv\u00e4gar, n\u00e4ra samarbete och ett \u00f6ppet klimat d\u00e4r erfarenheter och kunskap delas mellan kollegor. Vi ser positivt p\u00e5 att du vill beh\u00e5lla en klinisk f\u00f6rankring inom ditt medicinska specialistomr\u00e5de eller inom forskning, och \u00e4r d\u00e4rf\u00f6r \u00f6ppna f\u00f6r att diskutera tj\u00e4nstens omfattning.\nSom anst\u00e4lld omfattas du av kollektivavtal, och vi v\u00e4rnar om balans mellan arbete och privatliv genom bland annat flextid, friskv\u00e5rdsbidrag och gener\u00f6sa semestervillkor. \n\n\nL\u00e5ter det sp\u00e4nnande eller har du fr\u00e5gor? \nKontakta VD Suzanne Iverson Hemberg, suzanne.iverson.hemberg@ctc-ab.se  \nAns\u00f6kningstiden p\u00e5g\u00e5r till och med 14 september 2026. Tilltr\u00e4desdag enligt \u00f6verenskommelse.\nOm arbetsgivaren - CTC Clinical Trial Consultants AB\nCTC Clinical Trial Consultants AB \u00e4r en Clinical Research Organisation (CRO) med verksamhet i Uppsala, Stockholm, Link\u00f6ping och G\u00f6teborg.\nSom CRO utf\u00f6r vi kliniska studier p\u00e5 uppdrag av industrin och akademin och erbjuder ett komplett full-servicepaket av de tj\u00e4nster, moment och leveranser som kr\u00e4vs f\u00f6r att genomf\u00f6ra en klinisk pr\u00f6vning. Vi genomf\u00f6r idag studier fr\u00e5n tidig till sen fas (fas 0-IV).\nStudierna genomf\u00f6rs fr\u00e4mst p\u00e5 v\u00e5ra egna kliniker men ocks\u00e5 i samarbete med externa kliniker.\nHos oss arbetar ca 125 medarbetare varav cirka h\u00e4lften arbetar kliniskt. Huvudkontoret ligger i Uppsala.","price":null,"currency":"SEK","status":"active","noindex":false,"location":{"address":"Dag Hammarskj\u00f6ldsv\u00e4g 13","full_address":null,"city":"Uppsala","country":"SE","latitude":59.843849400852,"longitude":17.639556488241},"metadata":{"region":"Uppsala l\u00e4n","duration":"Tills vidare","employer":"CTC Clinical Trial Consultants AB","postcode":"75237","positions":1,"profession":"L\u00e4kare","salary_type":"Fast m\u00e5nads- vecko- eller timl\u00f6n","employer_url":"http:\/\/www.ctc-ab.se","scope_of_work":"100\u2013100 %","working_hours":"Heltid","employment_type":"Tillsvidareanst\u00e4llning (inkl. eventuell provanst\u00e4llning)","occupation_field":"H\u00e4lso- och sjukv\u00e5rd","employer_workplace":"CTC Uppsala","experience_required":true},"user_id":null,"is_sponsored":false,"views_count":0,"ai_views_count":2,"ai_vendor_counts":{"anthropic":2},"visibility":"public","submission_source":null,"submission_ai_name":null,"has_owner_email":true,"can_contact_owner":true,"phone":null,"owner_email":"suzanne.iverson.hemberg@ctc-ab.se","images":[],"published_at":"2026-08-17T14:29:35+00:00","expires_at":"2026-09-14T23:59:59+00:00","created_at":"2026-08-18T03:50:36+00:00","updated_at":"2026-08-19T02:46:25+00:00"}}