Senior Clinical Trial Manager
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Holbæk
Ensure advancement for a global clinical trial in phase 3
continues to expand locally and internationally, creating the need for expansion in the Clinical Operations department that aligns with a growing clinical trial portfolio. As the new Senior Clinical Trial Manager, you will report directly to the Senior Director, Head of Clinical Operations, and be responsbible for planning, oversight, and execution of a complex global clinical trial program in phase 3. This involves driving the full trial lifecyclefrom protocol development input, site and CRO/vendor selection and contracting to trial execution, close-out, and inspection readiness. All along ensuring seamless coordination across functional areas while maintaining alignment with project objectives and timelines. You will anticipate and identify potential risks early, developing and implementing mitigation strategies to safeguard timelines, budgets, and overall trial quality. Additionally, you will negotiate and manage study budgets with a focus on cost efficiency and value creation. Finally, the role involves close collaboration with both internal stakeholders as well as external providers to secure the advancement of clinical trials.
Experience with managing CRO globally in a fully outsourced setup
We expect you to hold a relevant bachelor's or master's degree, combined with extensive experience in the pharmaceutical industry, specifically within clinical operations management. Moreover, you have prior experience managing CROs and vendors on a global scale in a fully outsourced setup. In addition, you bring an excellent understanding and demonstrated application of Good Clinical Practice (GCP), ICH, and other relevant guidelines. You possess strong project management skills and the ability to lead and manage a wide range of internal and external stakeholders, exceling at meeting timelines and reaching corporate goals. Finally, fluency in English, written and spoken, is required.
Personally, you are proactive, energetic, and independent, thriving in an environment where you take ownership and set direction. You combine a performance-driven mindset with strong execution skills, enabling you to both define the framework and make it happen. Demonstrating excellent planning, coordination, and prioritization skills, you can work independently as well as collaboratively. Your robust professional foundation enables you to make timely and sound decisions, empowering you to effectively navigate through ambiguity and change.
Play a crucial role in an exciting international growth journey
This is your chance to embark upon a personal and organizational journey in a dynamic company where your know-how is greatly needed for the future development of . The recruitment process is carried out by Venaris Executive Search. For more information regarding the position, please reach out to Sr. Executive Search Consultant, Lars Nordlund, on +. All requests will be handled confidentially. If this position is for you, do not hesitate to apply by uploading your CV - it is not necessary to include a cover letter.
A/S is a global leader in carbohydrate chemistry and innovative treatments for iron deficiency and iron deficiency anaemia. Building on their foundational expertise in carbohydrate chemistry and cell cycle biology, they develop innovative treatments for unmet patient needs, with a focus on iron metabolism and blood-related disorders. Founded in 1965 and headquartered in Denmark, their team is made up of more than 700 specialists across the UK, Ireland, the Nordics, Germany, the USA, and China. Learn more about at www..com.
continues to expand locally and internationally, creating the need for expansion in the Clinical Operations department that aligns with a growing clinical trial portfolio. As the new Senior Clinical Trial Manager, you will report directly to the Senior Director, Head of Clinical Operations, and be responsbible for planning, oversight, and execution of a complex global clinical trial program in phase 3. This involves driving the full trial lifecyclefrom protocol development input, site and CRO/vendor selection and contracting to trial execution, close-out, and inspection readiness. All along ensuring seamless coordination across functional areas while maintaining alignment with project objectives and timelines. You will anticipate and identify potential risks early, developing and implementing mitigation strategies to safeguard timelines, budgets, and overall trial quality. Additionally, you will negotiate and manage study budgets with a focus on cost efficiency and value creation. Finally, the role involves close collaboration with both internal stakeholders as well as external providers to secure the advancement of clinical trials.
Experience with managing CRO globally in a fully outsourced setup
We expect you to hold a relevant bachelor's or master's degree, combined with extensive experience in the pharmaceutical industry, specifically within clinical operations management. Moreover, you have prior experience managing CROs and vendors on a global scale in a fully outsourced setup. In addition, you bring an excellent understanding and demonstrated application of Good Clinical Practice (GCP), ICH, and other relevant guidelines. You possess strong project management skills and the ability to lead and manage a wide range of internal and external stakeholders, exceling at meeting timelines and reaching corporate goals. Finally, fluency in English, written and spoken, is required.
Personally, you are proactive, energetic, and independent, thriving in an environment where you take ownership and set direction. You combine a performance-driven mindset with strong execution skills, enabling you to both define the framework and make it happen. Demonstrating excellent planning, coordination, and prioritization skills, you can work independently as well as collaboratively. Your robust professional foundation enables you to make timely and sound decisions, empowering you to effectively navigate through ambiguity and change.
Play a crucial role in an exciting international growth journey
This is your chance to embark upon a personal and organizational journey in a dynamic company where your know-how is greatly needed for the future development of . The recruitment process is carried out by Venaris Executive Search. For more information regarding the position, please reach out to Sr. Executive Search Consultant, Lars Nordlund, on +. All requests will be handled confidentially. If this position is for you, do not hesitate to apply by uploading your CV - it is not necessary to include a cover letter.
A/S is a global leader in carbohydrate chemistry and innovative treatments for iron deficiency and iron deficiency anaemia. Building on their foundational expertise in carbohydrate chemistry and cell cycle biology, they develop innovative treatments for unmet patient needs, with a focus on iron metabolism and blood-related disorders. Founded in 1965 and headquartered in Denmark, their team is made up of more than 700 specialists across the UK, Ireland, the Nordics, Germany, the USA, and China. Learn more about at www..com.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Holbæk.
Jobbet er oprettet på vores service den 17.9.2025, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Holbæk
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