27 Jobs für Clinical Drug Specialist
Stellenangebote Clinical Drug Specialist Jobs
Job gestern bei Mindmatch.ai gefunden
Rivia
• AT- 2 Lavamünd
About Rivia Rivia is a technology company building a data engine that powers the future of
clinical trial intelligence. Rivia was founded on the belief that new drugs can be [...]
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[...] brought to market more successfully with a fraction of todays capital. Biotechs are the source of most therapeutic innovation, yet clinical development is constantly constrained by fragmented data and outdated tooling. Rivia unifies clinical trial data at [. .. ] to significantly more efficient trial execution. In March 2026, Rivia raised its 15M Series A led by Earlybird Venture Capital. Rivias ambition is to become the standard infrastructure for modern drug development, transforming how trials are executed end-to-end. About the Role As Senior Infrastructure Engineer at Rivia, you own the AWS platform that everything runs on: EKS clusters, CI/ CD, identity, costs, backups, internal tooling. You are our first dedicated infrastructure hire, embedded in the engineering team and working [. .. ] Actions or equivalent) . An AInative way of working: you use agents (Claude Code or similar) for real infrastructure work and can show concrete examples. Comfortable being the only infrastructure specialist on the team: selfdirected, you find and fix problems without being asked. Bonus Keycloak or similar identity provider operations (OIDC, SSO, secrets management) . Spark or largescale data pipeline infrastructure experience. Exposure to regulated environments (ISO 27001, audit support) . Datadog or a comparable observability stack. Our Values At Rivia, [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Planet Pharma
Associate Director Biostatistics
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
We are seeking an experienced and highly motivated Associate Director,
Clinical Biomarker Biostatistics to play a pivotal role in advancing our clinical development and precision medicine strategies. This is an [...]
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[...] exciting opportunity for a strategic and handson biostatistician to drive the statistical leadership of biomarker initiatives across a diverse clinical portfolio. As a key member of the Biometrics organization, you will partner closely with Clinical Development, Translational Medicine, Bioinformatics, Biomarker Sciences, and Regulatory teams to develop and execute biomarker strategies that inform critical drug development decisions. You will provide both scientific leadership and technical expertise, ensuring robust statistical methodologies are applied throughout the biomarker lifecycle, from early clinical development through registration. Key Responsibilities Strategic Leadership Lead the statistical strategy for clinical biomarker development across multiple programs and therapeutic areas. Shape and influence biomarker plans [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
MSD
• AT- 2 Lavamünd
[. .. ] but that the site belongs to and is shaped by them. Our Schachen Biotech is a premier, state-of-the-art facility that integrates advanced technologies into the early-stage
clinical [...]
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[...] pipeline, refining them for future commercial launch. The site supports biologics drug substance manufacturing for early-phase clinical supply and serves as a hub for technology innovation and strategic advancement. The Compliance Excellence Specialist (P2) supports operational compliance and quality system activities for GMP biologics manufacturing at our Schachen. This role contributes to right-first-time execution, operational continuity, and inspection readiness by supporting investigations, documentation, change controls, risk records, and continuous improvement activities within assigned areas. Working with direction and guidance, the role [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
MSD
Specialist Upstream Operations (m/f/d)
• AT- 2 Lavamünd
[. .. ] they belong at Schachen, but that the site belongs to and is shaped by them. Our Schachen Biotech is a premier, stateoftheart facility that integrates advanced technologies [...]
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[...] into the earlystage clinical pipeline, refining them for future commercial launch. The site supports biologics drug substance manufacturing for earlyphase clinical supply and serves as a hub for technology innovation and strategic advancement. The Specialist Upstream Operations position requires fulltime physical presence at the site to support manufacturing and to enable optimal integration into an existing team. As a member of the growing manufacturing team at our company, you will be responsible for supporting various activities related to the implementation and GMP manufacturing of earlyphase [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Gouya Insights
• AT- 9 Wien
Looking for an opportunity to put your
clinical project management skills to the test? We are seeking an experienced Clinical Project Manager to join our team at Gouya Insights Gmb [...]
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[...] H Co KG, a clinical development consulting and clinical research services company supporting innovative biotech, pharmaceutical, and medical device companies. As Clinical Project Manager, you will take operational ownership of early-phase clinical studies and development projects, working at the interface between our clients, clinical sites, CROs, specialist vendors, and internal clinical development experts. You will translate clinical development strategies into operational execution, coordinate cross-functional project teams, and ensure timely delivery of projects within budget constraints, maintaining high quality and GCP standards. This role suits a proactive leader who enjoys taking ownership, working in a dynamic early-[. .. ] and other languages would be an advantage. A Bit About Us Founded in 2016, Gouya Insights is a clinical development consulting and clinical research services company dedicated to supporting innovative drug and medical device development. We work with biotech companies, startups, pharmaceutical companies, and medical device manufacturers to translate clinical development strategies into executable clinical programs and studies. Our expertise spans clinical and regulatory strategy, study design and scientific advice, clinical operations, CRO and vendor oversight, study conduct, and medical writing. [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
Country Clinical Research Lead
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
The IQVIA sponsor-dedicated
Clinical Functional Service Partnerships (Clinical FSP) department is supporting our clients project team in the execution of clinical trials. Joining the team provides the opportunity to [...]
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[...] manage clinical research projects in different therapeutic areas and to cooperate closely with one of our key clients. The country Clinical Research Lead (CRL) responsibilities [. .. ] and liaise with Clinical Study Teams and Global Monitoring, for Sponsors clinical studies conducted within country, ensuring key project milestones and high quality are delivered. Partner with local Study Startup Specialist or Clinical Research Associates to ensure consistency and accuracy of all core documents for local EC submission (i. e. submission pack, document customization, translations, quality check) . Act as the central point of contact for feasibilities in the country, for clinical studies when feasibilities are requested or deferred to country [. .. ] degree in life sciences, nursing or medical background preferred. Proven experience in feasibility and study start-up. Fluency in German and English language Demonstrated knowledge of clinical trial methodology and drug development process, related to monitoring clinical trials, GCP, SOP and country-specific regulatory requirements. Strong attitude to problem solving, effectively prioritize tasks and working independently. Effective organizational and time management skills. Ability to establish and maintain effective working relationships with co-workers, managers, internal and external stakeholders. Available for domestic [. .. ]
Job gestern bei Jobleads gefunden
Senior Infrastructure Engineer
• Lavamünd, Kärnten Lavamuend
About Rivia Rivia is a technology company building a data engine that powers the future of
clinical trial intelligence. Rivia was founded on the belief that new drugs can [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] be brought to market more successfully with a fraction of todays capital. Biotechs are the source of most therapeutic innovation, yet clinical development is constantly constrained by fragmented data and outdated tooling. Rivia unifies clinical trial data at [. .. ] to significantly more efficient trial execution. In March 2026, Rivia raised its 15M Series A led by Earlybird Venture Capital. Rivias ambition is to become the standard infrastructure for modern drug development, transforming how trials are executed end-to-end. About the Role As Senior Infrastructure Engineer at Rivia, you own the AWS platform that everything runs on: EKS clusters, CI/ CD, identity, costs, backups, internal tooling. You are our first dedicated infrastructure hire, embedded in the engineering team and working [. .. ] Actions or equivalent) . An AInative way of working: you use agents (Claude Code or similar) for real infrastructure work and can show concrete examples. Comfortable being the only infrastructure specialist on the team: selfdirected, you find and fix problems without being asked. Bonus Keycloak or similar identity provider operations (OIDC, SSO, secrets management) . Spark or largescale data pipeline infrastructure experience. Exposure to regulated environments (ISO 27001, audit support) . Datadog or a comparable observability stack. Our Values At Rivia, [. .. ]
Job gestern bei Jobleads gefunden
Director, Global Medical Safety Lead
• Genf
Führungs-/ Leitungspositionen
[. .. ] the business on a permanent basis. This is a hybrid role. Key Responsibilities: Act as the medical safety lead for assigned products, providing strategic pharmacovigilance and benefit-risk [...]
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[...] expertise across clinical, regulatory and cross-functional teams. Lead safety signal detection, evaluation and risk assessment activities, ensuring emerging safety data is reviewed and interpreted effectively. Chair or contribute to cross-functional safety review meetings and drive evidence-based decision making regarding product safety profiles. Support the development and execution of safety governance [. .. ] other stakeholders to ensure patient safety remains central to decision making. Key Requirements: MD, MBBS or equivalent medical degree. Significant pharmaceutical or biotechnology industry experience, including substantial experience within Pharmacovigilance/ Drug Safety. Demonstrated expertise in safety signal management, benefit-risk assessment and aggregate safety reporting. About Planet Pharma: Planet Pharma is an American parented Employment Business/ Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
[. .. ] stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management [...]
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[...] Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements Report contracting performance metrics and out of scope contracting activities as required. Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and [. .. ] site contracting experience Good negotiating and communication skills with ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of drug development process. Good understanding of clinical trial contract management. Fluent in English and German language IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Associate Director Biostatistics
• Lavamünd, Kärnten Lavamuend
Führungs-/ Leitungspositionen
We are seeking an experienced and highly motivated Associate Director,
Clinical Biomarker Biostatistics to play a pivotal role in advancing our clinical development and precision medicine strategies. This is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an exciting opportunity for a strategic and handson biostatistician to drive the statistical leadership of biomarker initiatives across a diverse clinical portfolio. As a key member of the Biometrics organization, you will partner closely with Clinical Development, Translational Medicine, Bioinformatics, Biomarker Sciences, and Regulatory teams to develop and execute biomarker strategies that inform critical drug development decisions. You will provide both scientific leadership and technical expertise, ensuring robust statistical methodologies are applied throughout the biomarker lifecycle, from early clinical development through registration. Key Responsibilities Strategic Leadership Lead the statistical strategy for clinical biomarker development across multiple programs and therapeutic areas. Shape and influence biomarker plans [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
[. .. ] issues, recurring problems, system dependencies, and institutional knowledge Support troubleshooting and escalation understanding Answer questions and provide clarification as the incoming employee assumes responsibility Coordinate with the [...]
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[...] Associate Dean for Clinical Services and College IT leadership to prioritize knowledge-transfer activities Perform other transition and training-related duties as assigned Requirements Bachelors degree or equivalent experience Final candidates are subject to successful completion of a background check A drug screen or physical may be required during the post offer process Core Competencies Demonstrates expertise in health systems administration training, focusing on knowledge transfer, system configurations, and operational support. Capable of developing documentation and providing orientation to new employees while coordinating with leadership for effective knowledge transfer. Highest-signal resume [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Clinical Applications Team Lead
Führungs-/ Leitungspositionen
Manage
Clinical Applications
Specialist project assignments and workload distribution Coordinate customer training schedules, go-lives, workflow assessments, and implementation activities Monitor project timelines, risks, and resource constraints Partner with [...]
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[...] Project Managers and cross-functional stakeholders to achieve implementation milestones Forecast resource needs and provide escalation support for complex customer situations Conduct site audits assessing [. .. ] support customer and team needs Must be legally authorized to work in the United States Employment visa sponsorship is not available now or in the future Successful completion of a drug screen, as applicable Desired: Nuclear Medicine Technologist (CNMT) , RT (N) , PET certification, or equivalent clinical credential Desired: Previous team lead, supervisor, mentoring, or people leadership experience Desired: Experience developing training programs, onboarding curricula, and process documentation Desired: Experience with quality improvement and operational excellence initiatives Core Competencies Demonstrates [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
• Sankt Gallen
Job Title: Senior
Specialist, Regulatory Affairs (EU/ Ro W) Job Type: Full time, Permanent Position CPL Life Sciences is collaborating with a growing biotechnology company focused on advancing innovative [...]
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[...] therapies for patients with unmet medical needs. We are seeking an experienced Senior Specialist, Regulatory Affairs (EU/ Ro W) to support global regulatory activities across development and [. .. ] dynamic and collaborative biotech environment. Key Responsibilities Support regulatory leads in the preparation, submission, and maintenance of regulatory applications across EU and Rest of World territories. Coordinate and contribute to Clinical Trial Applications (CTAs) , CTA amendments, pre-and post-authorisation submissions, and annual reports. Assist in the preparation, review, and submission of responses to questions from regulatory authorities. Participate in late stage development activities including initial and new MAAs and potentially any new indications. Ensure all regulatory submissions are complete, [. .. ] discipline. Advanced degree (MSc, Ph D, Pharm D, or equivalent) preferred. Experience Minimum of 4 years experience in Regulatory Affairs within the pharmaceutical, biotechnology, or health authority environment. Strong understanding of the drug development lifecycle and regulatory requirements across product development and commercialisation. Experience preparing and reviewing regulatory submissions including: Clinical Trial Applications (CTAs) Marketing Authorisation Applications (MAAs) Variations and lifecycle management submissions Experience interpreting and applying relevant ICH, EU, and international regulatory guidelines. Demonstrated ability to assess regulatory issues independently and provide [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
ASACS Counselor, Stuttgart, Germany
• Stuttgart, Baden- Württemberg
[. .. ] or family counseling as necessary. Promotes resiliency, reduces mental health disorders, reduces adolescent substance abuse, and develops general life skills through a proactive approach, such as engaging [...]
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[...] in community-wide drug awareness campaigns and interfacing with community key stakeholders including the garrison command on adolescent substance use issues and trends within the community. The job duties listed above are representative and not intended to be all-inclusive of what may be expected of an employee assigned to this job. A leader [. .. ] Requirements Masters degree from an accredited university (CACREP accreditation required for counseling programs) . Drug and Alcohol Certification (MRAS, CSAC, CAP, etc) . Licensed as an independent level provider Licensed Clinical Social Worker (LCSW) , Licensed Mental Health Counselor/ Licensed Professional Counselor (LHMC/ LPC) , Licensed Marriage and Family Therapist (LMFT) or Clinical/ Counseling Psychologist at Ph D level, with clinical license. Must be able to operate general office equipment including but not limited to: computer, phones and related media and information [. .. ] Marital and Family Therapist-Care Mgmt Care Mgmt, LMHC-Licensed Mental Health Counselor-Care Mgmt Care Mgmt, LPC-Licensed Professional Counselor-Care Mgmt Care Mgmt, MRAS-Masters Level Registered Addiction Specialist-Care Mgmt Care Mgmt, PSY-Psychologist-Care Mgmt Care Mgmt License And Certifications-Preferred : Salary Minimum : 58, 440 Salary Maximum : 93, 500 Salary Range Salary Minimum: 58, 440 Salary Maximum: 93, 500 This information reflects the anticipated base salary range for this position based on current national [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
• Vilseck, Bayern
[. .. ] or family counseling as necessary. Promotes resiliency, reduces mental health disorders, reduces adolescent substance abuse, and develops general life skills through a proactive approach, such as engaging [...]
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[...] in community-wide drug awareness campaigns and interfacing with community key stakeholders including the garrison command on adolescent substance use issues and trends within the community. The job duties listed above are representative and not intended to be all-inclusive of what may be expected of an employee assigned to this job. A leader [. .. ] Requirements Masters degree from an accredited university (CACREP accreditation required for counseling programs) . Drug and Alcohol Certification (MRAS, CSAC, CAP, etc) . Licensed as an independent level provider Licensed Clinical Social Worker (LCSW) , Licensed Mental Health Counselor/ Licensed Professional Counselor (LHMC/ LPC) , Licensed Marriage and Family Therapist (LMFT) or Clinical/ Counseling Psychologist at Ph D level, with clinical license. Must be able to operate general office equipment including but not limited to: computer, phones and related media and information [. .. ] Marital and Family Therapist-Care Mgmt Care Mgmt, LMHC-Licensed Mental Health Counselor-Care Mgmt Care Mgmt, LPC-Licensed Professional Counselor-Care Mgmt Care Mgmt, MRAS-Masters Level Registered Addiction Specialist-Care Mgmt Care Mgmt, PSY-Psychologist-Care Mgmt Care Mgmt Salary Range Salary Minimum: 58, 440 Salary Maximum: 93, 500 This information reflects the anticipated base salary range for this position based on current national data. Minimums and maximums may vary based on location. Actual pay will be adjusted based [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Clinical Application Specialist-Ultrasound-Region Bayern (All Genders)
Abgeschlossene Ausbildung
Firmenwagen Jobticket
Job Title
Clinical Application
Specialist-Ultrasound-Region Bayern (All Genders) Job Description Verantwortlich für den klinischen Support von Kunden vor und nach dem Verkauf im Ultraschall Business für den Süden [...]
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[...] von Deutschland, v. a. für das Gebiet Bayern. Dein Job Medizintechnische Geräte in ihrem jeweiligen Einsatzumfeld (Kliniken, Praxen, OPs, usw. ) beim Anwender demonstrieren und [. .. ] require accommodation in the job application process may contact 888-367-7223, option 5, for assistance. Philips is an Equal Employment and Opportunity Employer including Disability/ Vets and maintains a drug-free workplace. Know Your Rights #J-18808-Ljbffr 02932670 [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
ASACS Counselor, Vilseck, Germany
• Vilseck, Bayern
[. .. ] or family counseling as necessary. Promotes resiliency, reduces mental health disorders, reduces adolescent substance abuse, and develops general life skills through a proactive approach, such as engaging [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in community-wide drug awareness campaigns and interfacing with community key stakeholders including the garrison command on adolescent substance use issues and trends within the community. The job duties listed above are representative and not intended to be all-inclusive of what may be expected of an employee assigned to this job. A leader [. .. ] Requirements Masters degree from an accredited university (CACREP accreditation required for counseling programs) . Drug and Alcohol Certification (MRAS, CSAC, CAP, etc) . Licensed as an independent level provider Licensed Clinical Social Worker (LCSW) , Licensed Mental Health Counselor/ Licensed Professional Counselor (LHMC/ LPC) , Licensed Marriage and Family Therapist (LMFT) or Clinical/ Counseling Psychologist at Ph D level, with clinical license. Must be able to operate general office equipment including but not limited to: computer, phones and related media and information [. .. ] Marital and Family Therapist-Care Mgmt Care Mgmt, LMHC-Licensed Mental Health Counselor-Care Mgmt Care Mgmt, LPC-Licensed Professional Counselor-Care Mgmt Care Mgmt, MRAS-Masters Level Registered Addiction Specialist-Care Mgmt Care Mgmt, PSY-Psychologist-Care Mgmt Care Mgmt Salary Minimum 58, 440 Salary Maximum 93, 500 This information reflects the anticipated base salary range for this position based on current national data. Minimums and maximums may vary based on location. Actual pay will be adjusted based on an [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
ASACS Counselor, Kaiserslautern, Germany
• Kaiserslautern, Rheinland- Pfalz
[. .. ] or family counseling as necessary. Promotes resiliency, reduces mental health disorders, reduces adolescent substance abuse, and develops general life skills through a proactive approach, such as engaging [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in community-wide drug awareness campaigns and interfacing with community key stakeholders including the garrison command on adolescent substance use issues and trends within the community. The job duties listed above are representative and not intended to be all-inclusive of what may be expected of an employee assigned to this job. A leader [. .. ] Requirements Masters degree from an accredited university (CACREP accreditation required for counseling programs) . Drug and Alcohol Certification (MRAS, CSAC, CAP, etc) . Licensed as an independent level provider Licensed Clinical Social Worker (LCSW) , Licensed Mental Health Counselor/ Licensed Professional Counselor (LHMC/ LPC) , Licensed Marriage and Family Therapist (LMFT) or Clinical/ Counseling Psychologist at Ph D level, with clinical license. Must be able to operate general office equipment including but not limited to: computer, phones and related media and information [. .. ] Marital and Family Therapist-Care Mgmt Care Mgmt, LMHC-Licensed Mental Health Counselor-Care Mgmt Care Mgmt, LPC-Licensed Professional Counselor-Care Mgmt Care Mgmt, MRAS-Masters Level Registered Addiction Specialist-Care Mgmt Care Mgmt, PSY-Psychologist-Care Mgmt Care Mgmt Salary Range Salary Minimum: 58, 440 Salary Maximum: 93, 500 This information reflects the anticipated base salary range for this position based on current national data. Minimums and maximums may vary based on location. Actual pay will be adjusted based [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• Bayern
[. .. ] or family counseling as necessary. Promotes resiliency, reduces mental health disorders, reduces adolescent substance abuse, and develops general life skills through a proactive approach, such as engaging [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in community-wide drug awareness campaigns and interfacing with community key stakeholders including the garrison command on adolescent substance use issues and trends within the community. The job duties listed above are representative and not intended to be all-inclusive of what may be expected of an employee assigned to this job. A leader [. .. ] Requirements Masters degree from an accredited university (CACREP accreditation required for counseling programs) . Drug and Alcohol Certification (MRAS, CSAC, CAP, etc) . Licensed as an independent level provider Licensed Clinical Social Worker (LCSW) , Licensed Mental Health Counselor/ Licensed Professional Counselor (LHMC/ LPC) , Licensed Marriage and Family Therapist (LMFT) or Clinical/ Counseling Psychologist at Ph D level, with clinical license. Must be able to operate general office equipment including but not limited to: computer, phones and related media and information [. .. ] Marital and Family Therapist-Care Mgmt Care Mgmt, LMHC-Licensed Mental Health Counselor-Care Mgmt Care Mgmt, LPC-Licensed Professional Counselor-Care Mgmt Care Mgmt, MRAS-Masters Level Registered Addiction Specialist-Care Mgmt Care Mgmt, PSY-Psychologist-Care Mgmt Care Mgmt Salary Range Salary Minimum: 58, 440 Salary Maximum: 93, 500 This information reflects the anticipated base salary range for this position based on current national data. Minimums and maximums may vary based on location. Actual pay will be adjusted based [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
LAS Veterinarian (all genders)
• Hamburg
At Evotecs site in Hamburg, Germany, we are seeking a highly motivated and dedicated LAS Veterinarian (all genders) Pre-
clinical Research,
Drug Development and Biomarker Discovery Permanent, part time [...]
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[...] (min. 20h/ week) The Laboratory Animal Science (LAS) Veterinarian is responsible for overseeing the health, welfare, and humane use of laboratory animals, primarily mice and rats, within a CRO environment. This role ensures compliance with European and German regulatory standards while supporting pre-[. .. ] with legal and regulatory requirements Assume responsibility for the veterinary pharmacy Qualifications Doctorate in Veterinary Medicine (DVm/Dr. med. vet. ) ; board certification as a Veterinary Laboratory Animal Science specialist (Fachtierarzt für Versuchstierkunde) is highly desirable Sound knowledge of European and German animal welfare regulations, including Directive 2010/ 63/ EU, the German Animal Welfare Act (Tier Sch G) , and the 3Rs principle Strong communication skills and the ability to work effectively in multidisciplinary teams Excellent written and spoken German and [. .. ]
Job am 04.09.2026 bei Jobleads gefunden
Data Transparency Specialist Data Sharing, Anonymisation and Clinical Trial Disclosure (f/m/d-part/ full-time)
• München, Bayern
Your responsibilities will include Assessing data sharing requests, reviewing informed consent forms for data sharing feasibility Redaction of
clinical trial documents and anonymisation of individual patient data Preparing Redaction [...]
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[...] Proposal Document Packages (RPDP) for submission to EMA and Health Canada in compliance with EMA Policy 0070 and Health Canada PRCI Disclosure of clinical trial information for drugs and medical devices: Registering protocols and preparing results for submission to local [. .. ] regulations, and guidelines Communicate and coordinate with international study teams, act as a central point of contact Your profile University degree in data science or lifescience related discipline Knowledge of drug development and clinical science Experience in redaction of CCI and PPD in clinical documents is a plus Knowledge of EMA policy 0070 and Health Canada PRCI is a plus Experience in data anonymization and programming (e. g. , R/ SAS) is a plus Knowledge of the clinical trials disclosure regulatory [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Senior Specialist, Regulatory Affairs
[. .. ] Therapeutics, we are in rare for life. We continue to courageously forge new paths as we move toward a common goal of elevating science and service for [...]
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[...] rare patients. Senior Specialist, Regulatory Affairs (EU/ Ro W) Responsibilities Supports regulatory leads in the preparation, submission and maintenance of regulatory applications, including clinical trial applications (CTA) , routine CTA amendments, pre post authorization regulatory submissions and annual reports. Support regulatory leads in the preparation, review and submission of high-quality responses to questions to regulatory agencies. Ensures submissions are complete, properly formatted and comply with applicable regulatory requirements and timelines. Assist in interactions [. .. ] Equivalent combination of education and applicable job experience may be considered. 4+ years regulatory affairs experience in the pharmaceutical or biotechnology industry or government health agency. Good knowledge of the drug development process is required. Demonstrated ability to independently assess regulatory issues, evaluate multiple sources of information, exercise sound judgement and develop practical regulatory solutions. Experience in interpretation and application of ICH and EU guidelines relevant to product development and submission of pre/ post authorization applications. Experience in drafting and reviewing [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Clinical Research Associate II Sponsor-Dedicated FSP-Germany (m/f/d)
Homeoffice möglich
Clinical Research Associate II Sponsor-Dedicated FSP-Germany (m/f/d) Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Research Associate (Level II) Make an Impact at [...]
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[...] the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 [. .. ] manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i. e. , FSO, FSP, Government, etc. ) . Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role [. .. ] formal academic/ vocational qualification. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship. Valid drivers license where applicable. Knowledge, Skills and Abilities: Proven clinical monitoring skills Demonstrated understanding of medical/ therapeutic area knowledge and medical terminology Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations, and procedural documents Well-developed critical thinking skills, including but not [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Biotechnology Specialist, RDC Development
• Heidelberg, Baden- Württemberg
[. .. ] or pharmaceutical company work experience. We can also consider collaboration through consultancy/ part-time/ partnership ventures for particularly outstanding experts. This Role is Responsible For In-depth understanding of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] RDC drug design, synthesis, and analytical processes, and the ability to build specialized technical platforms. Ensure that projects are progressing and delivered on schedule. Leverage expertise in RDC drug design, synthesis, and analysis to build a quality technology platform to support our RDC-related services. Basic Qualifications Ph. D. in cellular biology, molecular biology, and biochemistry is preferred. Ph. D. in other related fields is also considered. In-depth knowledge of the scientific approach and clinical application of RDC based on chemical, medical, biological, and practical principles. Extensive work experience (3+ years of work experience) with in-depth expertise in the RDC field and the ability to solve professional problems in the R D process. Other Job Details Primary Location: New York, United States Employment Type: [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Senior Application Specialist-Life Science Research
• Freiburg im Breisgau, Baden- Württemberg
About Harvard Bioscience Harvard Bioscience is a leading developer, manufacturer and seller of technologies, products and services that enable fundamental research, discovery, and pre-
clinical testing for
drug development. [...]
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[...] Our customers range from renowned academic institutions and government laboratories to the worlds leading pharmaceutical, biotechnology and contract research organizations. With operations in North America, Europe, and China, we sell through a combination of direct and distribution channels to customers around the world. We are a publicly traded company [. .. ] significant organic growth by leveraging and expanding its deep customer relationships, new product development and an empowered, efficient sales force. THE OPPORTUNITY Harvard Bioscience is currently seeking a (Senior) Application Specialist Life Science Research for our March/ Freiburg office to provide expert application support for our physiological, cardiological, and respiratory research solutions. This role is focused on supporting national and international customers working with laboratory animal models, with particular emphasis on anesthesia, isolated organ systems, and perfusionbased applications. The Application Specialist [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Drug Specialist pro Jahr?
Als Clinical Drug Specialist verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Drug Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 27 offene Stellenanzeigen für Clinical Drug Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Drug Specialist Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Clinical Drug Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Drug Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Drug Specialist Stellenangebote:
- Planet Pharma (2 Jobs)
- MSD (2 Jobs)
- Rivia (1 Job)
- Gouya Insights (1 Job)
- PhD- Jobs. NET (1 Job)
In welchen Bundesländern werden die meisten Clinical Drug Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Drug Specialist Jobs werden derzeit in Bayern (5 Jobs), Baden-Württemberg (3 Jobs) und Hamburg (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Drug Specialist Jobs?
Clinical Drug Specialist Jobs gehören zum Berufsfeld Pharmazie.
