387 Jobs für Clinical Trials Management
Stellenangebote Clinical Trials Management Jobs
Job am 15.06.2025 bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] would be a plus if you also possess previous experience in: 3+ years Medical and Scientific Affairs experience. Expertise in coordinating and managing diagnostics studies in infectious [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] diseases in Germany. Clinical trials management to achieve timely completion of project deliverables. Biostatistics. Regulatory familiarity for using and managing on market diagnostics. Join our winning team today. Together, well accelerate the real-life impact of tomorrows science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting [. .. ]
Job vor 2 Tagen bei Neuvoo gefunden
Georgetown University in Qatar
Clinical Research Coordinator I
• Ingelheim am Rhein, Rhineland- Palatinate
Work-Life-Balance
[. .. ] with triaging phone calls and proactive patient communication. Coordinate collection of research specimens per protocol requirements. Schedule in-service training for appropriate staff on assigned clinical trials. Regularly [...]
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[...] update the Clinical Trials Management System (CTMS) with patient information and key dates to support responsible financial management of clinical trials. Collaborate with Data Manager (s) to assure documentation for the clinical trial is complete and accurate; assist with query resolution in a timely manner. Schedule/ facilitate sponsor meetings including PSV, SIV, MV Document and [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Roche
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] and ensure everyone has access to healthcare today and for generations to come. Join Roche where every voice matters. The Position Our Country Medical Director (CMD) drives [...]
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[...] scientific medical and clinical excellence and innovation through strategic leadership strong crossfunctional interactions and continuous engagement with the scientific community and key health care ecosystem this role you ensure medical compliance and superior patient outcomes while fostering a high performance culture and continuous professional development of the Medical team. Key Responsibilities As part of [. .. ] environments. Forwardthinking mindset innovative approach and excellent command of German and English Key Skills EMR Systems Post Residency Experience Occupational Health Experience Clinical Research Managed Care Primary Care Experience Medical Management Utilization Management Clinical Development Clinical Trials Leadership Experience Medicare We offer an annual salary starting from 120000 complemented by an attractive benefits package. This includes a competitive bonus scheme participation in our stock program pension contributions and more. Depending on your qualifications and experience a higher compensation is possible. You will also join an innovative and [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Novocure
Medical Science Liaison m/w/d-Austria
• AT- 9 Wien
[. .. ] patients treated with Tumor Treating Fields (TT Fields) . Additional responsibilities includebut are not limited toacting as a scientific interface between the company and HCP communities regarding [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] communication about Novocures clinical development plans as well as other research and development activities. Developing appropriate training materials, supporting external research projects related to marketed or investigational Novocure indications, and participating in field-based activities to advance existing products and introduce new indications are also part of the role. The MSL plays an important [. .. ] therapy awareness among prescribers and nonprescribers Manage the entire Austrian territory and all associated field activities Deliver medical training on Novocure products and disease areas Support and accompany investigator Sponsored Trials (ISTs) and other research projects Provide HCP insights and market information to the company Participate in medical (Europewide) congresses, and organize and follow up on advisory boards Promote scientific advancement related to TT Fields Support Phase 3 studies in collaboration with clinical teams and researchers Build and maintain relationships with [. .. ] in natural sciences, medicine, or engineering; an advanced scientific degree is an advantage At least 23 years of experience in a comparable medicalscientific role, ideally in oncology Experience in KOL management and/or investigator Sponsored Trials (ISTs) High willingness to travel (7080) and enthusiasm for proactive field work Ability to communicate scientific content confidently and tailored to the target audience Flexibility, independence, and sound judgment in dynamic environments Handson mentality and ability to collaborate in a small, dynamic team as well [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
ICON Strategic Solutions
• AT- 8 Gemeinde Au
[. .. ] are interested in managing the whole life cycle of the study from site selection to closeout, we want to hear from you. ICON plc is a worldleading [...]
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[...] healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking an experienced Clinical Research Associate II or Senior Clinical Research Associate (CRA) to join our diverse [. .. ] critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials of a single client by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. In this FSP program you will be working on cuttingedge Oncology trials and can take ownership of the full site management lifecycle. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with crossfunctional teams to ensure timely and accurate [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
ICON Strategic Solutions
Remote Senior CRA Oncology Trials Lead (Site Lifecycle)
• AT- 8 Gemeinde Au
Führungs-/ Leitungspositionen
A leading
clinical research organization is seeking a Senior Clinical Research Associate to oversee clinical trial activities, ensuring compliance and data integrity. The ideal candidate will have an advanced degree [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and extensive experience as a CRA, with excellent communication and problem-solving skills. This role involves site management of oncology trials and requires the ability to travel up to 60. A competitive salary and benefits are offered, including various health insurance options and flexible benefits. J-18808-Ljbffr 71022324 [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
F. Hoffmann- La Roche Gruppe
• AT- 9 Wien
Homeoffice möglich
[. .. ] authorities, patients, purchasers, and prescribers for Roches global Pharma Medicines Division. PDR is responsible for the timely submission of applications to health authorities. We also work closely [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the Submission Management Group (SMG) in Pharma Technical Regulatory (PTR) as a document and data hub for Quality documents. The Clinical Trial Regulatory Management Team enables the development of organizational and people capabilities of the future, we support and optimize the delivery of projects and initiatives to the organization both on the molecule and moleculeenabling portfolio. Global Labeling ensures the consistent and safe use of our medicines through highquality labels to [. .. ] Regulatory Submission, Clinical Trial and related Regulatory Operation areas to support our teams Help to build a knowledge base and leverage best practices in the area of Regulatory Submissions, Clinical Trials and supporting activities Develop your mentoring skills by training new joiners or other team members Continuously improve process efficiency and support service quality exercises Build a wide network within the operation groups to ensuring smooth operations in different teams Who you are We are looking for someone who is selfmotivated, [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
bio Mrieux
Medical Scientific Liaison (MSL) for Austria and Switzerland (m/f/d)
• AT- 9 Wien
[. .. ] care pathways and their needs in terms of unmet medical needs, medical information and medical education. Contribute to evidence generation by participating in company-sponsored postmarket studies, supporting [...]
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[...] Investigator Initiated Trials (IITs) in line with global strategy and according to Medtech requirements and bio Mrieux SOPs, and supporting clinical development initiatives including site identification, trial recruitment, registry and presentation of final approved data. Provide operational and medical support to marketing and sales teams (Account Managers, Clinical Education Managers, Business Developers) . Qualifications Academic degree in Medicine or Pharmacology. Advanced scientific degree (MD, Ph D, Pharm D) with relevant industry experience is [. .. ] the therapy area of infectious disease or intensive care is strongly preferred along with a solid professional reputation for interacting productively with healthcare professionals in the field. Experience in the management of clinical trials and Austrian and Swiss clinical research environment and legislation is desirable as well as experience in reviewing and analyzing scientific literature. Excellent oral and written communication and relationship building skills. Proactive approach with proven ability to take initiative and work both independently and as part of a [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
MSD
• AT- 9 Wien
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] D. degree required MPH, Ph. D. , MBA degree in Health Administration or Economics is seen as a plus Proven experience in global biopharmaceutical industry in Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Affairs and/or Clinical Development Solid people management experience running a large matrix organization of healthcare professionals Experience in one of the following fields : Oncology (strong plus) Infectious Diseases Treatment Vaccines or Specialty care Strong leadership skills demonstrated effective organizational skills including ability to set goals and align priorities Business acumen ethics and credible reputation with the [. .. ] date. Required Experience : Exec Key Skills : EMR Systems, Post Residency Experience, Occupational Health Experience, Clinical Research, Managed Care, Primary Care Experience, Medical Management, Utilization Management, Clinical Development, Clinical Trials, Leadership Experience, Medicare Employment Type : Full-Time Experience : years Vacancy : 1 J-18808-Ljbffr 70404421 [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
Blueprint Medicines, a Sanofi company
Field Medical Advisor, Alpine (Temporary)
• AT- 9 Wien
Homeoffice möglich
[. .. ] role in driving the success of Blueprints mission to improve and extend the lives of as many patients as possible through precision therapy. You will be a [...]
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[...] reliable bridge between clinical research market access and commercialization and within the overall organization building strong relationships and collaboration with external and internal stakeholders. As a Field Medical Advisor you will be living and sharing our core values and will be driven by the pursuit of new ideas new innovations and new ways of [. .. ] information officer for the corresponding indication and of clinical trial treatment plans and protocols of Phase IV projects in line with local compliance regulations. Supports interventional and non-Interventional clinical trials in close collaboration with with Clinical development Clinical Operations and Global Medical Affairs teams. Ensures a strategic approach to such programs and the development of clinical data to support the appropriate use of the Companys products. Works with colleagues of Blueprint Medicines International headquarter in Zug and other countries in [. .. ] commercial access medical and scientific needs on a local basis. Experience with product launches. Solid knowledge of country level regulations guidelines codes of practices and Access requirements Operational excellence : management skills planning prioritization decision making objective setting and plan execution. Strong customer orientation; science-based but good understanding of marketing needs; negotiation skills. Solid peer relationships with exposure to scientific and clinical experts with a demonstrated ability to engage internal and external leaders. Experience delivering effective and persuasive communications on [. .. ]
Job am 17.11.2025 bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
Experienced CRA Austria Syneos Health Application open. Position sought for Experienced
Clinical Research Associate in Austria. Description Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model places the customer and the patient at the center of [. .. ] their goals, and accelerate the delivery of therapies to change lives. Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culturewhere you can authentically be yourself. Our culture unites us globally and we dedicate ourselves to caring for our people. We continuously build the company we all want to work for and [. .. ] a centralized location. They conduct remote and onsite monitoring, automate data analytics and riskbased monitoring, and collaborate with site teams to implement effective quality monitoring processes that support successful clinical trials. Employment Details Seniority level: Mid Senior level Employment type: Fulltime Job function: Research, Analyst, and Information Technology Referrals increase your chances of interviewing at Syneos Health by 2x. Get notified about new Clinical Research Associate jobs in Vienna, Vienna, Austria. EEO Statement The Company is committed to compliance with the [. .. ]
Job am 03.11.2025 bei Mindmatch.ai gefunden
Takeda
In-Field Medical Manager (m/f/d)
• AT- 9 Wien
Homeoffice möglich
[. .. ] and identify opportunities to close data gaps. Deliver medical training to internal teams and provide scientific input into marketing strategies and pricing/ reimbursement dossiers. Oversee medical affairs [...]
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[...] activities, including budget management, internal knowledge transfer, and support for clinical trials and regulatory functions. What you bring: A scientific degree (MD, Pharmacy, or Life Sciences) or equivalent; relevant certifications and a valid driving license. Preferably over 2 years of experience in Medical Affairs or related roles, ideally with product launch exposure. Very good knowledge of English and German. Proven Medical Affairs [. .. ]
Job am 02.11.2025 bei Mindmatch.ai gefunden
Merck Healthcare
• AT- 9 Wien
Homeoffice möglich
[. .. ] regulatory activities, including any required Health Authority interactions for the Austrian organization, to ensure maintenance of Marketing Authorizations for the companys product portfolio. Your tasks will be [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the life cycle management of the marketed product as well as registration of new compounds, including possible Early Access Programs for new assets and relevant support for clinical trials as applicable. Who You Are You completed a university degree in pharmaceutical science (pharmacy, chemistry, biology, or related discipline) Minimum of 4 years of experience in the regulatory affairs field (RA proficiency) Experience and knowledge in review of promotional material and artworks You understand business needs, think strategically, and develop [. .. ]
Job am 02.11.2025 bei Mindmatch.ai gefunden
Octapharma Austria
Drug Safety Physician (m/f/d)
• AT- 9 Wien
[. .. ] and development location. Join us in shaping our vision to provide new health solutions advancing human life. Your Main Tasks And Responsibilities Conduct medical evaluations of cases [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] from spontaneous reports, clinical trials, and post-marketing surveillance to ensure compliance with applicable regulations and internal SOPs Assess the seriousness, listedness, and causality of individual case safety reports Initiate and support timely safety-related analyses Provide medical expertise for PBRERs/ PSURs and safety analyses Support the development and maintenance of Risk Management Plans and Risk Minimization Activities as needed Lead or contribute to signal management activities, including detection and evaluation for designated products Assist in creating and updating safety information, including product labeling for assigned products Your expertise and ideal skill set Medical doctor degree with a minimum of 3 years of [. .. ]
Job am 19.10.2025 bei Mindmatch.ai gefunden
Octapharma
• AT- 9 Wien
[. .. ] and development location. Join us in shaping our vision to provide new health solutions advancing human life. Your main tasks and responsibilities Conduct medical evaluations of cases [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] from spontaneous reports, clinical trials, and post-marketing surveillance to ensure compliance with applicable regulations and internal SOPs Assess the seriousness, listedness, and causality of individual case safety reports Initiate and support timely safety-related analyses Provide medical expertise for PBRERs/ PSURs and safety analyses Support the development and maintenance of Risk Management Plans and Risk Minimization Activities as needed Lead or contribute to signal management activities, including detection and evaluation for designated products Assist in creating and updating safety information, including product labeling for assigned products Your expertise and ideal skill set Medical doctor degree with a minimum of 3 years of [. .. ]
Job am 19.10.2025 bei Mindmatch.ai gefunden
Octapharma AG
Drug Safety Physician (m/f/d)
• AT- 9 Wien
[. .. ] and development location. Join us in shaping our vision to provide new health solutions advancing human life. Your main tasks and responsibilities Conduct medical evaluations of cases [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] from spontaneous reports, clinical trials, and post-marketing surveillance to ensure compliance with applicable regulations and internal SOPs Assess the seriousness, listedness, and causality of individual case safety reports Initiate and support timely safety-related analyses Provide medical expertise for PBRERs/ PSURs and safety analyses Support the development and maintenance of Risk Management Plans and Risk Minimization Activities as needed Lead or contribute to signal management activities, including detection and evaluation for designated products Assist in creating and updating safety information, including product labeling for assigned products Your expertise and ideal skill set Medical doctor degree with a minimum of 3 years of [. .. ]
Job am 14.10.2025 bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
2 days ago Be among the first 25 applicants Description CRA Austria Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] 000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company [. .. ] remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Induvidual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer [. .. ]
Job am 04.10.2025 bei Mindmatch.ai gefunden
SCARLETRED Holding GmbH
Customer Success Manager (f/m/d)
• AT- 9 Wien
[. .. ] edge AI-powered data analysis Services, that make it possible to standardize the process of skin imaging, objectify disease and treatment assessment, and to accelerate data collection and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] analysis in clinical trials and medical routine. We are growing and seeking new, experienced and hands-on team members who think outside of the box, deliver unique ideas and like to work in a fast-paced digital health and medical research environment. You are reliable, ambitious, your heart beats for clinical trials, digital health [. .. ] We are looking for a Customer Success Manager who has proven job experience in managing clinical trials, ideally also digital health project. In this job you will support our project management activities and foster our excellent communication with our clients and partners in biopharma, cosmetics and medical industry. You will act as a bridge to our customers and directly interact with C-level and report to our CEO. Responsibilities Manage running project and bring them to maximum success Estimate service requirements [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Bern
Führungs-/ Leitungspositionen
[. .. ] of the Executive Board role at Auriga Vision AG. Our client is the Swiss Cancer Institute (former SAKK) , a non-profit organization focused on the development and [...]
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[...] implementation of clinical trials in oncology based in Berne, Switzerland. As part of the teams expansion, we are looking for a Member of the executive Board. Responsibilities Leadership : Leading the Clinical Science team (Senior Scientific Director, Head of Clinical Development, Medical Science Liaison) , approximately 10 Clinical Scientists and Medical Advisors; active member of the Management Board for the Swiss organization, reporting to the CEO. Research Innovation : Translating projects into clinical trials; from study protocol to starting the clinical studies in Switzerland. Responsible for developing and implementing Investor Initiated Trials in Oncology in Switzerland Working closely with all leading oncology clinics across Switzerland. Scientific check [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Executive CSO-Oncology Trials Strategic Leadership
• Bern
Führungs-/ Leitungspositionen
A leading Swiss oncology research institute is seeking a Chief Scientific Officer (CSO) to lead the
Clinical Science team. This role involves developing and implementing clinical
trials, building [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] partnerships with the industry, and overseeing research innovations within Switzerland. The ideal candidate will have a medical or scientific background (Md/Ph D) , proven leadership experience, and fluency in English plus German and/or French. This is a unique opportunity to contribute significantly to the advancement of oncology research. [. .. ]
Job gestern bei Jobleads gefunden
Senior Product Manager, Observational Clinical Trials
• München, Bayern
About Us We are Carelane, an innovative, well-funded, and fully remote Health Tech company, revolutionising observational
clinical trials. By making them significantly faster to launch and easier to conduct, [...]
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[...] all at a fraction of the price, we unlock observational research at scale for non-enterprise-level clients. Through the democratisation of scientific research, we actually make the world a better place. At the heart of Carelane are our [. .. ] and analyse key metrics to measure product success, inform datadriven decisions, and demonstrate business impact. Stay current with regulatory changes affecting the clinical operations domain. Requirements 5+ years of Product Management experience and deep domain knowledge in clinical trial operations, gained from working at a pharmaceutical company, biotech, CRO, or a clinical technology provider. Deep expertise in key clinical trial technologies, especially e COA/ e PRO and e Consent. Proven track record of managing all stages of the product lifecycle and successfully launching products [. .. ]
Job gestern bei Jobleads gefunden
Senior Product Manager, Observational Clinical Trials
• Düsseldorf, Nordrhein- Westfalen Duesseldorf
About Us We are Carelane, an innovative, well-funded, and fully remote Health Tech company, revolutionising observational
clinical trials. By making them significantly faster to launch and easier to conduct, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] all at a fraction of the price, we unlock observational research at scale for non-enterprise-level clients. Through the democratisation of scientific research, we actually make the world a better place. At the heart of Carelane are our [. .. ] and analyse key metrics to measure product success, inform datadriven decisions, and demonstrate business impact. Stay current with regulatory changes affecting the clinical operations domain. Requirements 5+ years of Product Management experience and deep domain knowledge in clinical trial operations, gained from working at a pharmaceutical company, biotech, CRO, or a clinical technology provider. Deep expertise in key clinical trial technologies, especially e COA/ e PRO and e Consent. Proven track record of managing all stages of the product lifecycle and successfully launching products [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Lead Medical Director CVRm/Heart Failure
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The Position Roches Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development clinical strategies and plans that deliver medically differentiated therapies that provide meaningful improvement to patients. Roche is looking for an experienced and highly specialized individual to join the Cardiovascular, Renal, and Metabolism group. [. .. ] guiding and shaping our cardiovascular outcomes strategy. To be successful in this role, you will need to have extensive experience in late stage drug development and managing large-scale clinical trials, including outcome studies, in particular we are looking for candidates with experience in heart failure programs. You will have strong collaboration with cross-functional teams, including clinical research, regulatory affairs, and medical affairs, to ensure the successful progression of treatments through the pipeline and into the market. The position would [. .. ] understanding of cardiovascular diseases, clinical trial protocols, regulatory requirements, and possibly interactions with regulatory agencies to ensure studies meet the required standards. The Opportunity You will interact with high level management and experts both internally and externally, serving as internal consultants. You are expected to provide critical insights and contributions to the development and effectiveness of the assigned project. You have demonstrated a high level of experience in Clinical Development Plan (CDP) Strategy Planning, Execution, Regulatory Activities, and Cross-Functional Team [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Medical Science Liaison Ophta Nord
• München, Bayern
[. .. ] scientific exchange. Key Responsibilities Develop and maintain peertopeer collaborations and relationships with key medical experts in the ophthalmology community. Support medical affairs (e. g. , scientific exchange [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] conference support) and clinical development initiatives (e. g. , site identification, trial recruitment) . Collaborate with physicians on medical affairs initiatives including publications, advisory boards, medical education opportunities, and training. Serve as a scientific peertopeer resource to external disease experts and internal stakeholders. Support the medical community with uptodate medical information, robust disease expertise, [. .. ] communication skills in German and English. Energetically embraces responsibilities and demonstrates ability to achieve goals. Has strong initiative and functions well as part of a crossfunctional team. Exhibits excellent time management. Demonstrated ability to work independently. Experience in a startup environment preferred. Must be a proactive team player, flexible, and able to work in dynamic situations. Presentation Skills, Time Management, Clinical Research, Communication skills, GCP, Infusion Experience, Managed Care, Hospice Care, Conflict Management, Clinical Trials, Research Experience, Home Care Others Office is home based. Travel within region up to 75. Required travel to medical meetings, team meetings, and other group meetings (will require some weekends) . Benefits and Perks Apellis offers a comprehensive benefits package, flexible time off, summer and winter shutdowns, paid family leave, [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Lead Medical Director CVRm/Heart Failure
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. # # # # # The Position [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Roches Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development clinical strategies and plans that deliver medically differentiated therapies that provide meaningful improvement to patients. Roche is looking for an experienced and highly specialized individual to join the Cardiovascular, Renal, and Metabolism group. [. .. ] guiding and shaping our cardiovascular outcomes strategy. To be successful in this role, you will need to have extensive experience in late stage drug development and managing large-scale clinical trials, including outcome studies, in particular we are looking for candidates with experience in heart failure programs. You will have strong collaboration with cross-functional teams, including clinical research, regulatory affairs, and medical affairs, to ensure the successful progression of treatments through the pipeline and into the market. The position would [. .. ] requirements, and possibly interactions with regulatory agencies to ensure studies meet the required standards. # # # # # # The Opportunity You will interact with high level management and experts both internally and externally, serving as internal consultants You are expected to provide critical insights and contributions to the development and effectiveness of the assigned project You have demonstrated a high level of experience in Clinical Development Plan (CDP) Strategy Planning, Execution, Regulatory Activities, and Cross-Functional Team [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Management pro Jahr?
Als Clinical Trials Management verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Management Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 387 offene Stellenanzeigen für Clinical Trials Management Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Management Jobs?
Aktuell suchen 34 Unternehmen nach Bewerbern für Clinical Trials Management Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Management Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Management Stellenangebote:
- Tigermed (32 Jobs)
- Tubulis GmbH (21 Jobs)
- wax. (11 Jobs)
- Bio Talent (11 Jobs)
- Planet Pharma (10 Jobs)
- Carelane (10 Jobs)
In welchen Bundesländern werden die meisten Clinical Trials Management Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Management Jobs werden derzeit in Nordrhein-Westfalen (56 Jobs), Bayern (50 Jobs) und Berlin (27 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Management Jobs?
Clinical Trials Management Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
