30 Jobs für Pharmaceutical Writing in Nordrhein-Westfalen
Stellenangebote Pharmaceutical Writing in Nordrhein-Westfalen Jobs
Job vor 6 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
• Bergisch Gladbach
Beratungs-/ Consultingtätigkeiten Homeoffice möglich
[. .. ] audits, team trainings, and Qualifications You hold a university degree in engineering, life sciences, economics, informatics, or a related field. You bring experience in process design, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] documentation or manual writing as well as related project management-ideally within the pharmaceutical, logistics, or regulated environments. You have a strong analytical mindset and the ability to translate complex requirements into clear, actionable processes. You are a strong communicator who enjoys aligning with diverse stakeholders across functions and geographies and are comfortable with occasional business travel. Fluency in English is required; German is [. .. ]
Job vor 6 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
Senior Clinical Scientist Clinical Drug Development (m f d)
• Bergisch Gladbach
Homeoffice möglich
[. .. ] alignment from early research through late-stage clinical development. As an integral team member of Clinical Drug Development, you communicate complex scientific data clearly and effectively in English, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] both in writing and speaking, and leadership by coaching, mentoring, and educating less experienced colleagues while upholding high scientific and operational standards You hold an advanced degree (Ph D, MD, Pharm D, or equivalent) in life sciences, medicine, or a related field paired with significant experience in clinical development within the pharmaceutical or biotech industry, ideally including exposure to advanced therapy medicinal products (ATMPs) and/or CAR-T therapies. You have a proven track record in protocol development, regulatory submissions (IND, CTA, BLA, MAA) , and clinical data interpretation, and are recognized as an expert in the end-to-end process of [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Köln, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] and clinical knowledge in respective areas of Interest Your profile MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] and clinical knowledge in respective areas of Interest Your profile MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Dortmund, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] and clinical knowledge in respective areas of Interest Your profile MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Essen, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] and clinical knowledge in respective areas of Interest Your profile MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Essen, Nordrhein- Westfalen
[. .. ] Lead or Delegate Qualification Masters or Bachelors degree in a relevant discipline (e. g. , health economics, medicine, pharmacy, public health, epidemiology) Minimum 5 years experience in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the healthcare or pharmaceutical industry or consulting, working in the PRO field Hands on experience with PRO methodologies and operations across all phases of the product life cycle is preferred Track record of successful application of PROs with key external stakeholders such as FDA, EMA and relevant HTAs Knowledge and experience of Oncology therapy [. .. ] in a matrix organization, with proven ability to work cross-functionally, build coalitions and develop strong partnerships across functions Demonstrates strategic thinking and ability to travel up to 20 Outstanding writing and presentation skills and ability to work under pressure, to take accountability for business challenges, think strategically and tackle complex problems Intellectual curiosity and ability to identify trends and emerging patterns in areas such as PROs, Patient Experience Data, HEOR Requirements Start : 15.01.2025 Duration : 9 months [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Medical Affairs Manager
• Dortmund, Nordrhein- Westfalen
[. .. ] Lead or Delegate Qualification Masters or Bachelors degree in a relevant discipline (e. g. , health economics, medicine, pharmacy, public health, epidemiology) Minimum 5 years experience in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the healthcare or pharmaceutical industry or consulting, working in the PRO field Hands on experience with PRO methodologies and operations across all phases of the product life cycle is preferred Track record of successful application of PROs with key external stakeholders such as FDA, EMA and relevant HTAs Knowledge and experience of Oncology therapy [. .. ] in a matrix organization, with proven ability to work cross-functionally, build coalitions and develop strong partnerships across functions Demonstrates strategic thinking and ability to travel up to 20 Outstanding writing and presentation skills and ability to work under pressure, to take accountability for business challenges, think strategically and tackle complex problems Intellectual curiosity and ability to identify trends and emerging patterns in areas such as PROs, Patient Experience Data, HEOR Requirements Start : 15.01.2025 Duration : 9 months [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Medical Affairs Manager
• Düsseldorf, Nordrhein- Westfalen Duesseldorf
[. .. ] Lead or Delegate Qualification Masters or Bachelors degree in a relevant discipline (e. g. , health economics, medicine, pharmacy, public health, epidemiology) Minimum 5 years experience in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the healthcare or pharmaceutical industry or consulting, working in the PRO field Hands on experience with PRO methodologies and operations across all phases of the product life cycle is preferred Track record of successful application of PROs with key external stakeholders such as FDA, EMA and relevant HTAs Knowledge and experience of Oncology therapy [. .. ] in a matrix organization, with proven ability to work cross-functionally, build coalitions and develop strong partnerships across functions Demonstrates strategic thinking and ability to travel up to 20 Outstanding writing and presentation skills and ability to work under pressure, to take accountability for business challenges, think strategically and tackle complex problems Intellectual curiosity and ability to identify trends and emerging patterns in areas such as PROs, Patient Experience Data, HEOR Requirements Start : 15.01.2025 Duration : 9 months [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
• Bergisch Gladbach, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] and best practices. Qualifications Hold an advanced degree (Ph D, MD, Pharm D, or equivalent) in life sciences, medicine, or a related field paired with significant experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in clinical development within the pharmaceutical or biotech industry, ideally including exposure to ATMPs and/or CART therapies. Proven track record in protocol development, regulatory submissions (IND, CTA, BLA, MAA) , and clinical data interpretation, and recognized as an expert in the endtoend process of clinical data generation. Comprehensive expertise across the clinical data lifecycleworking backwards [. .. ] environment of internal stakeholders, external collaborators, and CRO partners to ensure alignment from early research through latestage clinical development. Communicate complex scientific data clearly and effectively in English, both in writing and speaking, and lead by coaching, mentoring, and educating less experienced colleagues while upholding high scientific and operational standards. What We Offer Free and selfdetermined time management, including mobile working. An intercultural environment characterized by diversity and flat hierarchies. Freedom to contribute creatively and play an active role in shaping [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
Senior Pre Sales Solutions Architect-Düsseldorf or Darmstadt, Germany
• Darmstadt, Hessen
[. .. ] bridge the gap between the business objectives and technical execution. You will be the primary technical leader for scientific end-users to design, architect, and deliver highly impactful [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] solutions to pharmaceutical and biotech customers. You will work to understand scientists and R D IT analysts needs, analyze their data environment, assist in the design and implementation of our solutions and enable customers to achieve faster ROI, reduced risk, smoother scaling, accelerated product adoption and ensure the long-term success of projects. [. .. ] to reach beneficial agreements. Technical Account Leadership Product Knowledge: Develop a deep understanding of the companys product or service offerings. Demo Development: Design and showcase tailored demonstrations to prospects. Proposal Writing: Contribute to RFPs/ RFIs with detailed technical specifications and solutions Project Management Timeline Management: Ensure projects are kept on track and within scope. Stakeholder Management: Coordinate with various stakeholders to ensure the smooth flow of presales activities. What You Have Done Scientific background academic and/or 5+ years professional experience [. .. ]
Job am 06.12.2025 bei Jobleads gefunden
Senior Pre Sales Solutions Architect-Düsseldorf or Darmstadt, Germany
• Düsseldorf, Nordrhein- Westfalen
[. .. ] bridge the gap between the business objectives and technical execution. You will be the primary technical leader for scientific end-users to design, architect, and deliver highly impactful [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] solutions to pharmaceutical and biotech customers. You will work to understand scientists and R D IT analysts needs, analyze their data environment, assist in the design and implementation of our solutions and enable customers to achieve faster ROI, reduced risk, smoother scaling, accelerated product adoption and ensure the long-term success of projects. [. .. ] to reach beneficial agreements. Technical Account Leadership Product Knowledge: Develop a deep understanding of the companys product or service offerings. Demo Development: Design and showcase tailored demonstrations to prospects. Proposal Writing: Contribute to RFPs/ RFIs with detailed technical specifications and solutions Project Management Timeline Management: Ensure projects are kept on track and within scope. Stakeholder Management: Coordinate with various stakeholders to ensure the smooth flow of presales activities. What You Have Done Scientific background academic and/or 5+ years professional experience [. .. ]
Job am 26.11.2025 bei Jobleads gefunden
• Mettmann, Nordrhein- Westfalen
[. .. ] natural sciences Experience: Several years in Medical Affairs, clinical development, or R D, ideally in neurology and/or rare diseases Expertise: Real-World Evidence, non-interventional research, publication planning, dossier [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] writing and scientific contribution to G-BA negotiations Knowledge: German regulatory requirements, AMNOG and HTA processes, ICH-GCP guidelines, local laws, and regulatory requirements Skills: Strategic thinking and scientific leadership Strong communication skills in German and English Ability to lead projects and collaborate cross-functionally Innovation mindset and digital affinity Integrity [. .. ] to adjustments; we will not be able to support you through this channel. Seniority level Mid-Senior level Employment type Full-time Job function Business Development and Project Management Industries Pharmaceutical Manufacturing and Biotechnology Research Referrals increase your chances of interviewing at UCB by 2x Get notified about new Strategy Manager jobs in Mettmann, North Rhine-Westphalia, Germany. Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-[. .. ]
Job am 25.11.2025 bei Jobleads gefunden
Process Design Expert (m f d)
• Bergisch Gladbach, Nordrhein- Westfalen
[. .. ] trainings, and training documentation. Qualifications You hold a university degree in engineering, life sciences, economics, informatics, or a related field. You bring experience in process design, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] documentation or manual writing as well as related project management ideally within the pharmaceutical, logistics, or regulated environments. You have a strong analytical mindset and the ability to translate complex requirements into clear, actionable processes. You are a strong communicator who enjoys aligning with diverse stakeholders across functions and geographies and are comfortable with occasional business travel. Fluency in English is required; German is [. .. ]
Job am 21.11.2025 bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Düsseldorf, Nordrhein- Westfalen
[. .. ] oversight of clinical studies including review and interpretation of clinical trial data and timely execution of deliverables in collaboration with relevant internal and external partners. Take a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lead role in writing protocol amendments, informed consents, and other protocolrelated documents for the operational execution of clinical studies. Participate in the startup of global clinical studies, working with Clinical Operations to ensure on schedule site activation and subject enrollment, monitoring, compliance with safety practices, policies, procedures as well as the daytoday management of [. .. ] a scientific discipline (i. e. MS, Pharm D, Ph D, MD) is preferred. A minimum of 3 years of clinical development research in oncology, or related clinical research experience within the industry (pharmaceutical, biotech, CRO) is required. Strong knowledge in clinical development in Oncology development is required. Significant experience with clinical evaluation projects including development of protocols, case report forms, informed consent and study initiation and monitoring. Significant experience with data integrity, exploration, analysis and presentation. Highperforming and energetic individual who demonstrates outstanding [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
• Nordrhein- Westfalen
[. .. ] direction based on scientific evidence Mentor junior scientists and contribute to the development of best practices in assay development and biotransformation studies WHO YOU ARE Ph. D. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in Biology, Chemistry, Pharmaceutical Sciences, or a related field Extensive experience in DMPK, with a focus on assay development in biotransformation, particularly metabolite identification from in vitro and in vivo studies; long-term experience in the pharmaceutical industry preferred Strong experience in high-resolution mass spectrometry and analytics A solid background in drug discovery [. .. ] of working collaboratively across departments Ability to manage multiple projects and priorities in a fastpaced environment Knowledge of relevant methodologies and technologies for biotransformation studies English fluent; verbally and in writing WHY BAYER? Our benefits package is flexible, appreciative, and tailored to your lifestyle, because: What matters to you, matters to us We ensure your financial stability through a competitive compensation package, consisting of an attractive base pay and our annual bonus. Whether its hybrid work models or parttime arrangements: Whenever [. .. ]
Job am 19.10.2025 bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Dortmund, Nordrhein- Westfalen
[. .. ] oversight of clinical studies including review and interpretation of clinical trial data and timely execution of deliverables in collaboration with relevant internal and external partners. Take a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lead role in writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Participate in the start-up of global clinical studies, working with Clinical Operations to ensure on schedule site activation and subject enrollment, monitoring, compliance with safety practices, policies, procedures as well as the day-[. .. ] a scientific discipline (i. e. MS, Pharm D, Ph D, MD) is preferred. A minimum of 3 years of clinical development research in oncology, or related clinical research experience within the industry (pharmaceutical, biotech, CRO) is required. Strong knowledge in clinical development in Oncology development is required. Significant experience with clinical evaluation projects including development of protocols, case report forms, informed consent and study initiation and monitoring. Significant experience with data integrity, exploration, analysis and presentation. High-performing and energetic individual who demonstrates [. .. ]
Job am 06.10.2025 bei Jobleads gefunden
Senior Process Quality Specialist 1
• Mettmann, Nordrhein- Westfalen
[. .. ] looking for the following education experience and skills Bachelors degree or higher in a relevant field (e. g. life sciences pharmacy medicine or law) . Or significant [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in the pharmaceutical industry preferably in quality management or clinical development. In-depth knowledge of international clinical quality standards and regulatory guidelines. Strong analytical problem-solving and project management skills. Excellent communication and interpersonal skills with fluency in English. Experience in writing and maintaining standard operating procedures is essential. Are you ready to go beyond to create value and make your mark for patients If this sounds like you then we would love to hear from you About us UCB is a global biopharmaceutical company focusing on neurology and immunology. We are [. .. ]
Job am 05.10.2025 bei Jobleads gefunden
• Essen, Nordrhein- Westfalen
[. .. ] oversight of clinical studies including review and interpretation of clinical trial data and timely execution of deliverables in collaboration with relevant internal and external partners. Take a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lead role in writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Participate in the start-up of global clinical studies, working with Clinical Operations to ensure on schedule site activation and subject enrollment, monitoring, compliance with safety practices, policies, procedures as well as the day-[. .. ] a scientific discipline (i. e. MS, Pharm D, Ph D, MD) is preferred. A minimum of 3 years of clinical development research in oncology, or related clinical research experience within the industry (pharmaceutical, biotech, CRO) is required. Strong knowledge in clinical development in Oncology development is required. Significant experience with clinical evaluation projects including development of protocols, case report forms, informed consent and study initiation and monitoring. Significant experience with data integrity, exploration, analysis and presentation. High-performing and energetic individual who demonstrates [. .. ]
Job vor 5 Tagen bei Neuvoo gefunden
West Pharmaceutical Services
Biological/ Chemical Laboratory Assistant (m/f/d) 1
• Stolberg (Rhineland) , North Rhine- Westphalia Stolberg (Rhineland)
[. .. ] Office) Experience in a GMP-regulated environment would be desirable Reliability, resilience, and ability to work in a team Careful and independent working style Good English skills in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] speaking and writing Working in shifts Preferred: Class B drivers license West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening. 73071468 [. .. ]
Job vor 13 Tagen bei Neuvoo gefunden
Miltenyi Biomedicine
Lead Clinical Scientist Drug Development (m f d)
• Bergisch Gladbach, North Rhine- Westphalia
Führungs-/ Leitungspositionen
[. .. ] best practices. Qualifications You hold an advanced degree (Ph D, MD, Pharm D, or equivalent) in life sciences, medicine, or a related field paired with significant experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in clinical development within the pharmaceutical or biotech industry, ideally including exposure to advanced therapy medicinal products (ATMPs) and/or CAR-T therapies. You have a proven track record in protocol development, regulatory submissions (IND, CTA, BLA, MAA) , and clinical data interpretation, and are recognized as an expert in the end-to-end process of [. .. ] alignment from early research through late-stage clinical development. As an integral team member of Clinical Drug Development, you communicate complex scientific data clearly and effectively in English, both in writing and speaking, and leadership by coaching, mentoring, and educating less experienced colleagues while upholding high scientific and operational standards. Additional Information What we offer Working with free and self-determined time management, also mobile working An intercultural environment characterized by diversity and flat hierarchies Freedom to contribute creatively and play [. .. ]
Job am 06.12.2025 bei Neuvoo gefunden
Tetra Science
• Düsseldorf, North Rhine- Westphalia
[. .. ] bridge the gap between the business objectives and technical execution. You will be the primary technical leader for scientific end-users to design, architect, and deliver highly impactful [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] solutions to pharmaceutical and biotech customers. You will work to understand scientists and R D IT analysts needs, analyze their data environment, assist in the design and implementation of our solutions and enable customers to achieve faster ROI, reduced risk, smoother scaling, accelerated product adoption and ensure the long-term success of projects. [. .. ] to reach beneficial agreements. Technical Account Leadership Product Knowledge: Develop a deep understanding of the companys product or service offerings. Demo Development: Design and showcase tailored demonstrations to prospects. Proposal Writing: Contribute to RFPs/ RFIs with detailed technical specifications and solutions Project Management Timeline Management: Ensure projects are kept on track and within scope. Stakeholder Management: Coordinate with various stakeholders to ensure the smooth flow of presales activities. Requirements What You Have Done Scientific background academic and/or 5+ years professional [. .. ]
Job am 05.12.2025 bei Neuvoo gefunden
Tetra Science
Senior Pre Sales Solutions Architect-Düsseldorf or Darmstadt, Germany
• Darmstadt, Hesse
[. .. ] bridge the gap between the business objectives and technical execution. You will be the primary technical leader for scientific end-users to design, architect, and deliver highly impactful [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] solutions to pharmaceutical and biotech customers. You will work to understand scientists and R D IT analysts needs, analyze their data environment, assist in the design and implementation of our solutions and enable customers to achieve faster ROI, reduced risk, smoother scaling, accelerated product adoption and ensure the long-term success of projects. [. .. ] to reach beneficial agreements. Technical Account Leadership Product Knowledge: Develop a deep understanding of the companys product or service offerings. Demo Development: Design and showcase tailored demonstrations to prospects. Proposal Writing: Contribute to RFPs/ RFIs with detailed technical specifications and solutions Project Management Timeline Management: Ensure projects are kept on track and within scope. Stakeholder Management: Coordinate with various stakeholders to ensure the smooth flow of presales activities. Requirements What You Have Done Scientific background academic and/or 5+ years professional [. .. ]
Job am 03.12.2025 bei Neuvoo gefunden
UCB
Sales Representative Hidradenitis Suppurativa (m/f/d)
• Voerde, North Rhine- Westphalia
[. .. ] methods Use all available analytical tools, including Digital Assistant, Advanced Analytics, Omnichannel Customer Journey, Persona Segmentation Interested? Were Looking for the following qualifications, experience, and skills: Completed [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] training as a pharmaceutical sales representative and/or a degree in a scientific field Several years of experience in specialty and hospital sales; experience with biologics is a plus Excellent ability to communicate complex medical information High level of personal responsibility, integrity, and discretion Fluent in German; English proficiency in speaking and writing flexibility and willingness to stay overnight due to the size of the area Permanent residence in the advertised area Are you ready to go beyond to create value and make your mark for patients? If this sounds like you, then we would love to hear from you 71346602 [. .. ]
Job am 11.11.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Associate Medical Director/ Medical Director
• Essen
Führungs-/ Leitungspositionen
[. .. ] clinical knowledge in respective areas of Interest Your profile Qualifications: MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
1 von 2Weiter » Weitere Suchergebnisse laden »
Häufig gestellte Fragen
Wieviel verdient man als Pharmaceutical Writing pro Jahr?
Als Pharmaceutical Writing verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmaceutical Writing Jobs in Nordrhein-Westfalen bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 30 offene Stellenanzeigen für Pharmaceutical Writing Jobs in Nordrhein-Westfalen.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Writing Jobs in Nordrhein-Westfalen?
Aktuell suchen 7 Unternehmen nach Bewerbern für Pharmaceutical Writing Jobs in Nordrhein-Westfalen.
Welche Unternehmen suchen nach Bewerbern für Pharmaceutical Writing Stellenangebote in Nordrhein-Westfalen?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmaceutical Writing Stellenangebote in Nordrhein-Westfalen:
- Tubulis GmbH (6 Jobs)
- Miltenyi Biotec B. V. Co. KG (2 Jobs)
- Tetra Science (2 Jobs)
- West Pharmaceutical Services (1 Job)
- Miltenyi Biomedicine (1 Job)
- UCB (1 Job)
Zu welchem Berufsfeld gehören Pharmaceutical Writing Jobs in Nordrhein-Westfalen?
Pharmaceutical Writing Jobs in Nordrhein-Westfalen gehören zum Berufsfeld Technische Dokumentation / Redaktion.
