Wir verwenden Cookies, um die Benutzererfahrung zu verbessern, den Verkehr zu analysieren und relevante Anzeigen anzuzeigen.
Mehr Annehmen
Position eingeben

Gehaltsübersicht für Clinical Trial in Schweiz

Erhalten Sie Statistikinformationen per E-Mail

Gehaltsübersicht für Clinical Trial in Schweiz

14 875 ₣ Durchschnittliches Monatsgehalt

Durchschnittliches Gehaltsniveau in den letzten 12 Monaten: "Clinical Trial in Schweiz"

Währung: CHF USD Jahr: 2021
Das Balkendiagramm zeigt die Änderung des Gehaltsniveaus in der Clinical Trial Branche in Schweiz

Verteilung des Stellenangebots "Clinical Trial" in Schweiz

Währung: CHF
Wie die Grafik zeigt, in Schweiz gilt Kanton Neuenburg als die Region mit der größten Zahl der offenen Stellen in und an zweiter Stelle folgt Basel-Stadt. Den dritten Platz nimmt Kanton Waadt ein.

Ranking der Kantone in Schweiz gemäß dem Gehaltsniveau für den Beruf "Clinical Trial"

Währung: CHF
Laut der Statistik unserer Webseite ist Clinical Trial der bestbezahlte Beruf in Kanton Zug. Die Fachkraft verdient durchschnittlich 21333 CHF. Als nächstes folgt Basel-Stadt and Basel-Landschaft.

Ranking der ähnlichen Stellenangebote gemäß dem Gehaltsniveau in Schweiz

Währung: CHF
Unter den ähnlichen Berufen in Schweiz gilt Röntgen als der bestbezahlte Beruf. Laut unserer Webseite beträgt das Durchschnittseinkommen 49967 CHF. An zweiter Stelle folgt Chefarzt mit dem Gehalt von 32667 CHF und den dritten Platz nimmt Oberarzt mit dem Gehalt von 25214 CHF ein.

Empfohlene Stellenangebote

Senior Clinical Trial Manager (CTM, Phase III) – Project Team Leader
Coopers Group AG, Basel-Stadt
Leading, planning, and delivering clinical trials Phase III in Oncology & / or Infectious disease , to ensure that studies are carried out according to protocols, SOPs, regulations and principles of GCP. From start-up to close out.Lead the cross functional study team dedicated to the clinical study to ensure clinical program goals and timelines are metManage operational aspects of projects including budgeting, study initiation and risk managementSelect and manage external vendors, such as CROs, central laboratories ...Ensure the delivery of the clinical study according to ICH GCPProvide operational & scientific input into Protocol synopsis, Study protocol and all other study related documentsParticipate to due diligence activitiesYour profileMSc or PhD degree in Biotechnology, Biology, Microbiology or Life Sciences related mattersMin of 8-10+ years' experience with proven track record of international clinical trials management (Phase III) in the Pharmaceutical Industry, biotech & / or CRO. Previous monitoring experience requiredSuccessful candidate must provide sound experience in Phase III clinical trial in Oncology (& / or Haematology & / or Infectious disease): mandatorySound expertise in the implementation and use of EDC, IWRS, eTMF, CTMS and any other digital clinical trial systems.Excellent experience in management of CROs, vendors and consultantsProven track record in project management skills & team resources allocation and coordinationFluent in English Only the profiles matching the requirements will be considered (#PHASE III ONCOLOGY). Successful candidate must provide a FULL DOSSIER IN ENGLISH
Clinical Trial Manager
Coopers Group AG, Basel-Stadt
 Your responsibilities will be but not limited to:Clinical trial material (CTM) label review and approval and assisting with CTM forecasting.Proactively identifying and resolving operational issues/processes to ensure achievement of study milestones, data quality and data integrity; escalates study-related issues appropriately in a timely manner.Participating in data cleaning, listing, and report output reviews.Developing, reviews, and approves study-related manuals, plans, specifications, charters, newsletters, and materials.Protocol deviation listing reviews and meetings.Responsible for oversight of study budget, investigator and vendor contracts, budgets and payments.Protocol, table, figure, data listings and clinical study report reviews. Experience:University degree in life-sciencesMin 5 years of experience in a similar position in phase IIIExperience in rare diseases  
Senior Clinical Trial Physician, Oncology
Bristol Myers Squibb Company, Boudry, Switzerland
Senior Clinical Trial Physician, Oncology At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Functional Area Description The Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. Position Summary / Objective Serves as a primary source of medical accountability and oversight for multiple clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 - Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Position Responsibilities Medical Monitoring Contributes to and is a key member of a high performing Study Delivery Team (SDT) and may be a member of the Clinical Development Team (CDT) Leads medical data review of trial data, including eligibility review Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management guidelines) Holds responsibility for assessment of key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives Leads collaboration with CS and inputs into protocols, providing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related clinical considerations) Fulfills GCP and compliance obligations for clinical conduct and maintains all required training Clinical Development Expertise & Strategy In collaboration with the Clinical Development Lead, designs and develops clinical plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets Provides oversight and medical accountability for a group of studies Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment working with Clinical Scientists (CS) Partners with CS to support executional delivery of studies (e.g., site activation, enrollment status, as well as adjudication for protocol violations, significant, non-significant deviations etc.) Identifies and builds relationships with principal investigators. Identifies and cultivates thought leaders in order to gain their inputs on emerging science in drug and biomarker research, disease knowledge, and design of clinical development studies and programs Maintains a strong medical/scientific reputation within the disease area. Has in-depth knowledge of etiology, natural history, diagnosis, and treatment of the disorder. Holds strong expertise in the disease area by attending scientific conferences and ongoing review of the literature Keeps abreast of development and regulatory issues related to other competitive or relevant compounds in development and how our portfolio fits into the competitive landscape Provides ongoing medical education in partnership with collaborating Clinical Scientists to allow for protocol-specific training, supporting the study team, investigators, and others Health Authority Interactions & Publications Contributes to and serves as medical point of expertise in key Health Authority interactions and advisory board meetings as Clinical Trial Physician Authors/drafts clinical content for CSRs, regulatory reports, briefing books and submission documents to support closure, clinical narratives, reporting and filling of the study in partnership with CSs Degree Requirements MD required (or x-US equivalent) Experience Requirements 5 or more years of clinical trial experience, either in industry or academic setting is required Key Competency Requirements Ability to communicate information clearly and lead presentations in scientific and clinical settings Subspecialty training in applicable therapeutic area desired Expertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation Expertise in drug development process Expertise in the components needed to execute an effective clinical plan and protocols Strong leadership skills with proven ability to lead and work effectively in a team environment Travel Required Domestic and International travel may be required. Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture. To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S. Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to
Sr. Clinical Trial Physician, Acute Myeloid Leukemia
Bristol Myers Squibb Company, Boudry, Switzerland
Sr. Clinical Trial Physician, Acute Myeloid Leukemia At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. The Sr. Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. Position Summary / Objective Serves as a primary source of medical accountability and oversight for multiple clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 - Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Position Responsibilities Medical Monitoring Contributes to and is a key member of a high performing Study Delivery Team (SDT) and may be a member of the Clinical Development Team (CDT) Leads medical data review of trial data, including eligibility review Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management guidelines) Holds responsibility for assessment of key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives Leads collaboration with CS and inputs into protocols, providing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related clinical considerations) Fulfills GCP and compliance obligations for clinical conduct and maintains all required training Clinical Development Expertise & Strategy In collaboration with the Clinical Development Lead, designs and develops clinical plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets Provides oversight and medical accountability for a group of studies Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment working with Clinical Scientists (CS) Partners with CS to support executional delivery of studies (e.g., site activation, enrollment status, as well as adjudication for protocol violations, significant, non-significant deviations etc.) Identifies and builds relationships with principal investigators. Identifies and cultivates thought leaders in order to gain their inputs on emerging science in drug and biomarker research, disease knowledge, and design of clinical development studies and programs Maintains a strong medical/scientific reputation within the disease area. Has in-depth knowledge of etiology, natural history, diagnosis, and treatment of the disorder. Holds strong expertise in the disease area by attending scientific conferences and ongoing review of the literature Keeps abreast of development and regulatory issues related to other competitive or relevant compounds in development and how our portfolio fits into the competitive landscape Provides ongoing medical education in partnership with collaborating Clinical Scientists to allow for protocol-specific training, supporting the study team, investigators, and others Health Authority Interactions & Publications Contributes to and serves as medical point of expertise in key Health Authority interactions and advisory board meetings as Clinical Trial Physician Authors/drafts clinical content for CSRs, regulatory reports, briefing books and submission documents to support closure, clinical narratives, reporting and filling of the study in partnership with CSs Degree Requirements MD required (or x-US equivalent) Experience Requirements 5 or more years of Industry experience and/or clinical trials experience is required Key Competency Requirements Ability to communicate information clearly and lead presentations in scientific and clinical settings Subspecialty training in applicable therapeutic area desired Expertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation Expertise in drug development process Expertise in the components needed to execute an effective clinical plan and protocols Strong leadership skills with proven ability to lead and work effectively in a team environment Travel Required Domestic and International travel may be required. Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture. To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S. Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to
Senior Clinical Trial Physician, Oncology
Bristol Myers Squibb Company, Boudry, Switzerland
Senior Clinical Trial Physician, Oncology At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. The Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. Position Summary / Objective Serves as a primary source of medical accountability and oversight for multiple clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 - Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Position Responsibilities Medical Monitoring Contributes to and is a key member of a high performing Study Delivery Team (SDT) and may be a member of the Clinical Development Team (CDT) Leads medical data review of trial data, including eligibility review Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management guidelines) Holds responsibility for assessment of key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives Leads collaboration with CS and inputs into protocols, providing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related clinical considerations) Fulfills GCP and compliance obligations for clinical conduct and maintains all required training Clinical Development Expertise & Strategy In collaboration with the Clinical Development Lead, designs and develops clinical plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets Provides oversight and medical accountability for a group of studies Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment working with Clinical Scientists (CS) Partners with CS to support executional delivery of studies (e.g., site activation, enrollment status, as well as adjudication for protocol violations, significant, non-significant deviations etc.) Identifies and builds relationships with principal investigators. Identifies and cultivates thought leaders in order to gain their inputs on emerging science in drug and biomarker research, disease knowledge, and design of clinical development studies and programs Maintains a strong medical/scientific reputation within the disease area. Has in-depth knowledge of etiology, natural history, diagnosis, and treatment of the disorder. Holds strong expertise in the disease area by attending scientific conferences and ongoing review of the literature Keeps abreast of development and regulatory issues related to other competitive or relevant compounds in development and how our portfolio fits into the competitive landscape Provides ongoing medical education in partnership with collaborating Clinical Scientists to allow for protocol-specific training, supporting the study team, investigators, and others Health Authority Interactions & Publications Contributes to and serves as medical point of expertise in key Health Authority interactions and advisory board meetings as Clinical Trial Physician Authors/drafts clinical content for CSRs, regulatory reports, briefing books and submission documents to support closure, clinical narratives, reporting and filling of the study in partnership with CSs Degree Requirements MD required (or x-US equivalent) Experience Requirements 5 or more years of clinical trial experience, either in industry or academic setting is required Key Competency Requirements Ability to communicate information clearly and lead presentations in scientific and clinical settings Subspecialty training in applicable therapeutic area desired Expertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation Expertise in drug development process Expertise in the components needed to execute an effective clinical plan and protocols Strong leadership skills with proven ability to lead and work effectively in a team environment Travel Required Domestic and International travel may be required. BMSPHY, BMSONCRD Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture. To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S. Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to
Clinical Trial Physician
Randstad (Schweiz) AG, Allschwil
Do you want to work in a big pharmaceutical company? Are you a medical doctor? Do you have experiences in Clinical Trial? You should then read the following lines!Our client, based in the Basel area, is looking for a Clinical Trial Physician for a one year contract.All tasks below should be performed in compliance with Good Clinical Practices and SOP’s.The CTP is a member of the Clinical Trial Team (CTT). The tasks and activities of the CTP are carried out in close collaboration with the Clinical Trial Scientist (CTS) for the trial related activities and with the Clinical Project Physician (CPP) and Clinical Project Scientist (CPS) for the project related activities.Key Responsibilities:• Developing a sound understanding of the science and medicine relating to Neuroscience• Developing a sound understanding of the complexity of global clinical development with a particular attention to methodological and ethical aspects of development, in the assigned therapeutic area (Neuroscience)• Performing literature reviews, and write position papers as necessary.• Contribute to writing of Protocol and Core Informed Consent Form (CICF), including amendments• Input into the Clinical Study Report (CSR).• Medical training of the Clinical Trial Team (CTT) members and/or staff .• Medical oversight of the study (including safety, quality and performance of the trial).• Clinical Trial results interpretation.• Involved in the organization and management of the following external activities: Contacts with external Experts, Steering Committees (SC), Independent Data Monitoring Committees (IDMC), other study or project committees.• Answering to trial-related EC/IRB and HA questions.• Ensuring that the Case Report Form is designed to allow careful and comprehensive collection of data.Requirements:• MEDICAL DOCTOR• At least 4 year- experience in clinical research in a Pharmaceutical or Biotech company or equivalent in Academia• Clinical research or Clinical experience in the indication relevant to the Clinical Project is preferred (multiple sclerosis)• Good knowledge of drug development and clinical trial process based on previous experience• Good knowledge of regulatory requirements/ICH guidelines• Good organizational skills, able to work as part of a team and independently• Good communication skills• Detailed oriented• Fluent in English Do not waste any minutes, apply now! We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.
Senior Clinical Trial Physician, Acute Myeloid Leukemia
, Boudry
At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. The Sr. Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical
Clinical Trial Physician, Hematology
, Boudry
At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. The Sr. Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical
Clinical Trial Coordinator (CTC) or Assistant (CTA)
Hamilton Bonaduz AG - Hamilton Medical AG – Hamilton Storage GmbH, Bonaduz, CH
Hamilton Medical is a dynamic, internationally successful medical device company headquartered in Bonaduz, Switzerland. At Hamilton Medical, we live for ventilation technology. Technology that helps caregivers improve the lives of their critically ill patients. We believe that innovation is essential to meet the demands of critical care.To strengthen our multinational team, we are looking for motivated people in all areas of the company: from software developers to medical or healthcare professionals, from engineers to export specialists, from production workers to regulatory affairs specialists, and from project leaders to product managersResponsibilities:Support project teams in all administrative aspects around clinical trials including but not limited to:Document management in accordance with the applicable guidelines for clinical studies - Good Documentation Practices (GCP)Set up and maintain clinical investigator files and documentationCollaborate with Clinical Trial Leads, set up systems for filing; collect, track and distribute clinical study documentsCoordinate internal and external stakeholders, facilitating smooth processes and top qualityEnter and maintain data into selected study tracking databases and ensure a high level of data qualityCreate and maintain systems for study device distribution, traceability and inventory controlParticipate in projects or initiatives on request, or take on department-wide tasks to contribute to the optimization of processes related to clinical trialsQualifications:High School Diploma and a minimum of 4 years of related experience (CTA), or Associated higher education (office management, administration, finance, health care, life science or similar preferred) and a minimum of 2 years of related experience (CTC)Excellent communication skills in business fluent German and English - verbal and written.Good knowledge of MS Office, familiar with common computer applications such as word processing and spreadsheets and have knowledge of document filing systems is a plusFamiliarity with clinical research / trial processes and international regulations (ICH, GCP etc.)Excellent organizational and project management skills with a keen attention to detail and a high sense of accountabilityMotivated and reliable team player, but also able to work independentlyStrong interpersonal skills are a mustDetail and quality orientedAre you interested? Then please apply online. For further inquiries, please contact us at
Clinical Trial Manager (Homebased - Europe) - Iqvia Biotech
, Basel
Job description IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment. The sector we are in is cutting edge for therapies with un-met medical need. Clinical Trial Managers at IQVIA Biotech are responsible for the planning, implementation and execution of contracted clinical monitoring activities. They are functionally responsible for all clinical monitoring team members throughout the duration of each clinical trial. Responsibilities of this role include: * Working closely with the Project Manager to define programme targets for clinical monitoring staff and ensure work is d