8 Jobs für Medical Trials in Mainz
Stellenangebote Medical Trials in Mainz Jobs
Job vor 13 Tagen bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
Mainz, Germany full time Job ID: 11231 About the Role As an Associate Director Scientific/
Medical Writing, you will play a pivotal role in advancing Bio NTechs mission to revolutionize [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medicine by ensuring the timely creation of highquality scientific and regulatory documents. Your contributions will directly impact the development and approval of novel therapeutic agents, supporting Bio NTechs efforts to address diseases with high medical needs. Collaborating within [. .. ] medical writer in the pharmaceutical/ biotech industry. Prior experience: drafting documents for multiple indications, preferably in Bio NTechrelevant indications. drafting alone new or updated CTPs and CSRs required for Phase IIII trials. drafting low to medium complexity variants of the following (new or updated variants) : IBs, clinical CTD modules, DSURs/ Annual Reports, RMPs, Response documents, Diversity Plans, PIPs/ PSPs, and other CTD Module1 documents. editing/ reviewing R D reports. drafting (from source data) low to medium complexity variants of R D [. .. ]
Job gestern bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
[. .. ] you will collaborate closely with the VP of Clinical Development to drive innovative strategies for assigned programs. In this pivotal role, you will oversee the design and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] execution of clinical trials across all phases, ensuring data integrity, patient safety, and regulatory approval. Leveraging your deep expertise in Immuno-Oncology and Oncology, you will lead matrix teams to deliver impactful results while guiding decisions with scientific rigor and medical insight. Join us to shape the future of medicine through cutting-edge research and development. Your Contribution Lead clinical trial design to develop plans for new compounds from early exploratory studies through late-stage development and regulatory approval. Collaborate with the VP to operationalize clinical strategies for assigned portfolios and [. .. ]
Job gestern bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
[. .. ] and Associate Directors Clinical Trial Management Plan resources for the team in alignment with Senior Director, Clinical Operations Govern CROs and vendors while contributing to strategic sourcing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] decisions for clinical trials A Good Match: University degree or experience in a medical profession (e. g. , Nurse or Medical Technical Assistant) 12+ years of experience in project management, regulatory submissions, and global study organizations, including 6+ years leading global clinical development teams At least 4 years of recent Oncology experience within the past 7 years (phase 2 or 3) as a Lead [. .. ]
Job gestern bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
[. .. ] you will collaborate closely with the VP of Clinical Development to drive innovative strategies for assigned programs. In this pivotal role, you will oversee the design and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] execution of clinical trials across all phases, ensuring data integrity, patient safety, and regulatory approval. Leveraging your deep expertise in Immuno-Oncology and Oncology, you will lead matrix teams to deliver impactful results while guiding decisions with scientific rigor and medical insight. Join us to shape the future of medicine through cutting-edge research and development. Your Contribution Lead clinical trial design to develop plans for new compounds from early exploratory studies through late-stage development and regulatory approval. Collaborate with the VP to operationalize clinical strategies for assigned portfolios and [. .. ]
Job gestern bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
The Associate Director, Safety Sciences provides scientific expertise for
medical safety tasks. Core responsibilities include safety data review and analysis from different sources, periodic report authoring and the oversight of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the safety surveillance activities for the assigned program (s) . The Safety Scientist ensures that all processes are conducted according to Bio NTech s written procedures, laws and regulations. The Associate [. .. ] in close collaboration with the Safety Physician to author relevant safety sections of clinical trial documents for the assigned program (s) . Your Contribution: Perform cumulative safety data reviews across trials or programs to assess safety profiles and identify emerging risks or trends Oversee the Safety Surveillance activities, including signal detection, literature reviews, and aggregate safety data analysis using tools like Safety Dashboards, Spotfire, and Elluminate Collaborate with Safety Physicians to review and align on safety data conclusions for informed decision-[. .. ]
Job gestern bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
[. .. ] forefront of steering clinical strategies and their operationalization for assigned programs. This role directly contributes to Bio NTech s mission by leading the strategic direction of platforms [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and programs, ensuring clinical trials are designed and executed with precision from early to late-stage development through regulatory approval. You will work within a dynamic team environment, collaborating closely with multidisciplinary teams globally to drive innovation, ensure patient safety, and uphold data integrity. Your Contribution: Lead and manage a team of medical professionals representing Clinical Development within global teams, including Core Teams, Project Teams, and Study Teams. Oversee the design and execution of clinical trials, ensuring alignment with Bio NTechs strategic goals and regulatory requirements. Supervise the creation of integrated evidence generation plans paving paths toward regulatory approval. Represent Bio NTech in collaborations with [. .. ]
Job gestern bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
Are you passionate about advancing medicine to unlock the full potential of the immune system against infectious diseases? Join Bio NTech as a
Medical Director in Clinical Development and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] play a key role in defining and executing the global development strategy for cutting-edge programs. Reporting to the VP of Clinical Development for Infectious Diseases, you will lead a cross-functional team to drive innovation in the design and execution of clinical trials that impact patient lives and shape Bio NTechs rapidly expanding pipeline. This exciting role offers the unique opportunity to contribute to our mission while thriving in a dynamic and fast-paced environment. Your contribution: In this role, you will: Define the strategy and oversee the global execution of assigned Infectious Diseases [. .. ]
Job gestern bei Jooble gefunden
Biontech
Associate Director Scientific/ Medical Writing
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
As an Associate Director Scientific/
Medical Writing, you will play a pivotal role in advancing Bio NTechs mission to revolutionize medicine by ensuring the timely creation of high-quality scientific [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and regulatory documents. Your contributions will directly impact the development and approval of novel therapeutic agents, supporting Bio NTech s efforts to address diseases with high medical needs. [. .. ] in the pharmaceutical/ biotech industry. Prior experience:-drafting documents for multiple indications, preferably in Bio NTech-relevant indications. drafting alone new or updated CTPs and CSRs required for Phase I-III trials. drafting low to medium complexity variants of the following (new or updated variants) : IBs, clinical CTD modules, DSURs/ Annual Reports, RMPs, Response documents, Diversity Plans, PIPs/ PSPs, and other CTD Module 1 documents. editing/ reviewing R D reports. drafting (from source data) low to medium complexity variants of R [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Medical Trials pro Jahr?
Als Medical Trials verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Medical Trials Jobs in Mainz bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 8 offene Stellenanzeigen für Medical Trials Jobs in Mainz.
Zu welchem Berufsfeld gehören Medical Trials Jobs in Mainz?
Medical Trials Jobs in Mainz gehören zum Berufsfeld Forschung, Lehre, Wissenschaft.
