Clinical Drug Specialist Stellenangebote

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42 Stellenangebote

Stellenangebote Clinical Drug Specialist Jobs bei Jobleads

Job vom 17.06.2024

Director, Advisory Consulting/ Biopharmaceutical Sector

• München, Bayern Führungs-/ Leitungspositionen Beratungs-/ Consultingtätigkeiten

MEHR

Director, Advisory Consulting/ Biopharmaceutical Sector Our client is a specialist advisory firm with a global footprint, focused on helping biopharmaceutical clients create clinical and commercial strategies that deliver differentiated and valuable brands. Having recently expanded their global footprint with a new subsidiary company [...] both new and existing accounts. As your clients will mainly be in the US, the Director position requires a thorough understanding of the evolving US biopharma market and trends. Many projects will also involve global client stakeholders; therefore, knowledge of drug development and commercialization in other markets is also desirable. Time Allocation: 75 of your time will be spent in office, [...]
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Stellenangebote Clinical Drug Specialist Jobs bei StepStone

Job vom 05.11.2024 Formycon AG Senior IT Infrastructure/ IT Operations Specialist (gn) • Martinsried/ Planegg Beratungs-/ Consultingtätigkeiten Homeoffice möglich

MEHR

Formycon AG sucht in Martinsried/ Planegg eine/n Senior IT Infrastructure/ IT Operations Specialist (gn) (ID- Nummer: 11665849) . Formycon is an international leading, independent developer of high- quality biopharmaceutical medicines, especially biosimilars. With an experienced team comprised of around 240 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process. Our focus is on treatments in ophthalmology and immunology as well as for other [...]

Stellenangebote Clinical Drug Specialist Jobs bei Freelance.de

Job vom 16.10.2024

Für Freelancer- Clinical Trial Associate/ Specialist (CTA/ CTA)

• München Freiberuflich

MEHR

Freelancer Projekt- Sie haben Erfahrung als Clinical Trial Associate/ Specialist (CTA/ CTA) und suchen den Sprung zu einem namhaften Pharmaunternehmen iin München? Dann dürfte folgende Stelle sehr interessant für Sie [...] aller organisatorischen und administrativer Aufgaben Gute Englisch- und EDV- Kenntnisse Haben Sie Interesse an dieser Position? Dann freue ich mich auf Ihre Bewerbung und ein interessantes Gespräch mit Ihnen Stichworte: Pharmazie, Pharma, Medizin, Freelance, freiberuflich, befristet, Medical, Biologie, Onkologie, Orphan, drug, Master, Bachelor, GCP, GxP, Clinical, CRO, Studien, klinisch, TMF, Prüfplan, Prüfbogen, Monitor, CRA, CTA, Clinical Research Associate. Trial Master File; [...]
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Job vom 16.10.2024 Für Freelancer- Associate Clinical Project Manager (Biotech) m/w/d • München Freiberuflich

MEHR

Freelancer Projekt- Sie haben Erfahrung als Clinical Trial Associate/ Specialist (CTA/ CTA) und suchen den Sprung zu einem namhaften Pharmaunternehmen iin München? Dann dürfte folgende Stelle sehr interessant für Sie [...] administrativer Aufgaben Gute Englisch- und EDV- Kenntnisse Haben Sie Interesse an dieser Position? Dann freue ich mich auf Ihre Bewerbung und ein interessantes Gespräch mit Ihnen Rückfragen gerne telefonisch. Stichworte: Pharmazie, Pharma, Medizin, Freelance, freiberuflich, befristet, Medical, Biologie, Onkologie, Orphan, drug, Master, Bachelor, GCP, GxP, Clinical, CRO, Studien, klinisch, TMF, Prüfplan, Prüfbogen, Monitor, CRA, CTA, Clinical Research Associate. Trial Master File; [...]

Job vom 26.09.2024

Für Freelancer- Clinical Trial Associate/ Specialist (CTA/ CTS)

• München Freiberuflich

MEHR

Freelancer Projekt- Sie haben Erfahrung als Clinical Trial Associate/ Specialist (CTA/ CTS) und suchen den Sprung zu einem namhaften Pharmaunternehmen iin München? Dann dürfte folgende Stelle sehr interessant für Sie [...] administrativer Aufgaben Gute Englisch- und EDV- Kenntnisse Haben Sie Interesse an dieser Position? Dann freue ich mich auf Ihre Bewerbung und ein interessantes Gespräch mit Ihnen Rückfragen gerne telefonisch. Stichworte: Pharmazie, Pharma, Medizin, Freelance, freiberuflich, befristet, Medical, Biologie, Onkologie, Orphan, drug, Master, Bachelor, GCP, GxP, Clinical, CRO, Studien, klinisch, TMF, Prüfplan, Prüfbogen, Monitor, CRA, CTA, Clinical Research Associate. Trial Master File; [...]
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Weitere Stellenangebote Clinical Drug Specialist bei Jobleads

Neu Job vor 7 Std. gefunden Associate Director, Oncology Therapeutic Group Führungs-/ Leitungspositionen

MEHR

[...] global/ regional requirements at all stages of the product life cycle. Why you? Basic Qualifications Skills: We are looking for professionals with these required skills to achieve our goals: Bachelor s degree in biological or healthcare science. Experience in the drug development process within regulatory affairs. Proven ability to manage development, submission, and approval activities in different regions globally. Ability to develop necessary specialist knowledge for the product in a specific oncology disease area. Preferred Qualifications Skills: Please note the following skills are not [...] have them, please still apply: Advanced Scientific Degree (PhD, MD, PharmD) . Knowledge of all phases of the drug development process in regulatory affairs. Capability to lead regional development, submission, and approval activities in local region (s) . Knowledge of clinical trial and licensing requirements in all major countries in the region and, ideally, knowledge of other key Agency processes globally. [...]
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Neu Job vor 7 Std. gefunden

Director Regulatory Affairs Oncology, early stage (m/f/x)

• München, Bayern Führungs-/ Leitungspositionen

MEHR

To provide European regulatory strategy support for assigned projects, products and non- project work. Act as a specialist in the area of oncology. Represent Regulatory Affairs internally working on a collaborative basis both within Europe and globally as [...] expertise on regulatory matters. Represent Regulatory Affairs in external interactions (e. g. authorities, affiliates, partners, CROs) providing expertise on regulatory strategy to achieve regional and global goals. Roles Responsibilities: European regulatory strategy support for assigned projects, covering product development plans, clinical trials and Marketing Authorizations Applications (MAA) as well as product life cycle management European Regulatory Affairs representation on global project [...] Pharmacy, Master and/ or PhD preferred; Master Degree in Regulatory Affairs is a plus Minimum of 10 years of experience in the pharmaceutical industry and minimum of 8 years of experience in global regulatory affairs with emphasis on early stage drug development and marketing authorization applications in Europe, experience with clinical trials, orphan drugs and paediatric clinical development Experience of working [...]

Job gestern gefunden Director Regulatory Affairs Oncology, early stage (m/f/x) • München, Bayern Führungs-/ Leitungspositionen

MEHR

[...] for people with cancer. Our European headquarters are in Munich, Germany, and we have affiliates in 13 European countries and Canada. The Position: To provide European regulatory strategy support for assigned projects, products and non- project work. Act as a specialist in the area of oncology. Represent Regulatory Affairs internally working on a collaborative basis both within Europe and globally as [...] team, providing expertise on regulatory matters. Represent Regulatory Affairs in external interactions (e. g. authorities, affiliates, partners, CROs) providing expertise on regulatory strategy to achieve regional and global goals. European regulatory strategy support for assigned projects, covering product development plans, clinical trials and Marketing Authorizations Applications (MAA) as well as product life cycle management. European Regulatory Affairs representation on global project [...] Pharmacy, Master and/ or PhD preferred; Master Degree in Regulatory Affairs is a plus. Minimum of 10 years of experience in the pharmaceutical industry and minimum of 8 years of experience in global regulatory affairs with emphasis on early stage drug development and marketing authorization applications in Europe, experience with clinical trials, orphan drugs and paediatric clinical development. Experience of working [...]

Job gestern gefunden

Associate Director, Oncology Therapeutic Group

• Baar, Zug Führungs-/ Leitungspositionen

MEHR

[...] regions globally. Implement regional strategies in support of global projects. Ensure compliance with global/ regional requirements at all stages of the product life cycle. Why you? Basic Qualifications Skills: Bachelor s degree in biological or healthcare science. Experience in the drug development process within regulatory affairs. Proven ability to manage development, submission, and approval activities in different regions globally. Ability to develop necessary specialist knowledge for the product in a specific oncology disease area. Preferred Qualifications Skills: Advanced Scientific Degree (PhD, MD, PharmD) . Knowledge of all phases of the drug development process in regulatory affairs. Capability to lead regional development, submission, and approval activities in local region (s) . Knowledge of clinical trial and licensing requirements in all major countries in the region and, ideally, knowledge of other key Agency processes globally. [...]

Job gestern gefunden Global Regulatory Affairs Director- Oncology Führungs-/ Leitungspositionen

MEHR

[...] Bachelor s degree in biological or healthcare science Extensive experience in pharmaceutical industry Regulatory Affairs Proven track record of interactions with Health Authorities Capable of leading development, submission and approval activities in different region (s) globally Ability to develop necessary specialist knowledge for the product in a specific oncology disease area. Preferred Qualifications Skills: Advanced Scientific Degree (PhD, MD, PharmD) . Knowledge of the drug development process in regulatory affairs. Awareness of global regulatory processes, including submission and approval activities. Understanding of clinical trial and licensing requirements. Strong matrix working skills with the ability to facilitate dialogue and contribute to strategic changes. Creative [...]

Job gestern gefunden

Global Regulatory Affairs Director- Oncology

• Baar, Zug Führungs-/ Leitungspositionen

MEHR

[...] Bachelor s degree in biological or healthcare science. Extensive experience in pharmaceutical industry Regulatory Affairs. Proven track record of interactions with Health Authorities. Capable of leading development, submission and approval activities in different region (s) globally. Ability to develop necessary specialist knowledge for the product in a specific oncology disease area. Preferred Qualifications Skills: Advanced Scientific Degree (PhD, MD, PharmD) . Knowledge of the drug development process in regulatory affairs. Awareness of global regulatory processes, including submission and approval activities. Understanding of clinical trial and licensing requirements. Strong matrix working skills with the ability to facilitate dialogue and contribute to strategic changes. Creative [...]

Job vor 4 Tagen gefunden Laboratory Associate Regulated Bioanalysis • Basel, Basel- Stadt

MEHR

[...] immunogenicity, safety and PD (soluble target and biomarkers) endpoints and ensures assay readiness, data context enabling decision making and ultimately deliver robust and fit for purpose regulatory filings. The Opportunity This position is an excellent opportunity for a talented Laboratory Specialist to integrate into a dynamic lab team dedicated to the support of pre- clinical and clinical projects when complex bioanalytical assays or time- critical data are required. As part of the pRED organization you continuously participate in improving processes. You validate bioanalytical assays for the quantification of novel therapeutic proteins, soluble targets, biomarkers, or the detection of anti- drug antibodies, fulfilling project requirements and complying with international guidance. You support pre- clinical and clinical phase I/ II/ III studies [...]

Job vor 4 Tagen gefunden

Laboratory Associate Regulated Bioanalysis

• Basel, Basel- Stadt

MEHR

Job vor 6 Tagen gefunden VP Clinical Development

MEHR

Job Description Job Title: VP Clinical Development- Oncology Tasks Responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and take clinical development [...] Core Clinical Trial Protocols and Pediatric Development Plans together with your cross- functional project teams. Mentor a team of Clinical Program Leads. Provide input to Project Analysis Data Management Plans, Company Core Data Sheet, Annual Safety Report/ IND (Investigational New Drug) Safety Reports. Provide medical leadership in regulatory meetings and support submission strategy, regulatory dossiers, and safety issues. Maintain an external [...] asset (s) , e. g. , Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. Oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry. Successful [...]

Job vor 6 Tagen gefunden

Executive Director Clinical Development

Führungs-/ Leitungspositionen

MEHR

Job Description Job Title: Executive Director Clinical Development- Oncology Tasks Responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and take clinical development [...] Core Clinical Trial Protocols, and Pediatric Development Plans together with your cross- functional project teams. Mentor a team of Clinical Program Leads. Provide input to Project Analysis Data Management Plans, Company Core Data Sheet, Annual Safety Report/ IND (Investigational New Drug) Safety Reports. Provide medical leadership in regulatory meetings and support submission strategy, regulatory dossiers, and safety issues. Maintain an external [...] for your designated asset (s) , including Health Authorities, Key External Experts, Associations, Patient groups, and Payers. Oversee and support all contacts to external experts, executive/ steering committees, adjudication committees, and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) several years of experience in the pharmaceutical industry. Successful [...]

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Stellenangebote Clinical Drug Specialist Jobs bei Job-Consult

Job vom 11.09.2024 PhD- Jobs. NET Specialist Adult Psychiatry • Schweden/ sonstiges/ Europa

MEHR

specialist adult psychiatry phd jobs net schweden description of the work at the clinic health center we are looking for three [...] you are expected to have at least visits per day supervision of younger colleagues is included as a natural part of the work and participation in the units medical development specialists perform the most physician specific tasks such as diagnostics drug treatment and the establishment of a care treatment plan together with the team on the other hand psychotherapies are conducted [...] via skype and preferably look forward to your interest in participating in the development of this we also wish you to have an interest in adhd treatment and substitution treatment for opiate addiction number of vacancies education specialist education psychiatry clinical experience what kind of treatments patients do you expect the doctor to have experience with years of experience all of [...]

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