Ref #: 38151
Employment type: Permanent - Full-Time
Location: Homebased, Germany
Posted: 09-Jun-2022
Description
If you are seeking a career where you can truly make a difference in the lives of others, then here is your chance. ICON is hiring a Senior Manager of Clinical Operations (m/f/d) to work closely together with one of the most successful pharmaceutical companies in the world. If you are a Clinical Project- or Program Manager with high expertise in line– and client management anywhere in Germany willing to work home based and open for a new challenge, we would like to get to know you.
Key responsibilities:
• To lead and support the Management Team, while managing the client’s demands.
• To assist our client in performing oversight in fulfilling its site management activities and obligations in relation to clinical studies as the primary sponsor of those studies.
• Create a culture of process improvement with a focus on streamlining processes adding value to business and meeting our client’s needs
• Travel (approximately 50%) in Germany
• Interact with strategic partners (KOLs, Investigators and Site Staff) as necessary for execution of clinical trials and reinforcement of the company’s brand
• Ensure that staff achieve expected quality compliance standards
• Support staff to achieve delivery of study objectives
• Provide leadership in the continuous improvement in performance
• Support staff with action plan development and resolution of findings from Clinical Quality Assurance audits
• Conduct resource planning and metrics review with site management
• Conduct staff regular performance assessments and personal/career discussions with direct reports
• Responsible for providing regular updates to Director level Management and adhering to metrics
Education & Experience
• Profound knowledge of clinical trial processes and operations in Germany
• Familiar with ICH/GCP guidelines
• Several years of strong experience as a Project- and/or Program Manager
• Attention to detail, organizational skills, time management & prioritization
• Strong personality with great leadership and people skills
• Relationship management & influencing skills as well as presentation skills
• Proficiency in English and German
What is offered:
• 100% home based
• Interesting trials in various therapeutic areas.
• Unlimited employment contract with ICON
• Contribution to pension scheme
• Working exclusively with one client
• Position responsibility is planned to be extended to additional countries
Why this vacancy is right for you:
We offer an exciting and challenging work environment for clinical research professionals looking for an opportunity to contribute to the success of a company dedicated to researching, developing, manufacturing and marketing pharmaceuticals that improve health and quality of life.
Interested? Please submit your CV to nadine.rabenstein@docsglobal.com. We are looking forward to getting to know you.
Key responsibilities:
• To lead and support the Management Team, while managing the client’s demands.
• To assist our client in performing oversight in fulfilling its site management activities and obligations in relation to clinical studies as the primary sponsor of those studies.
• Create a culture of process improvement with a focus on streamlining processes adding value to business and meeting our client’s needs
• Travel (approximately 50%) in Germany
• Interact with strategic partners (KOLs, Investigators and Site Staff) as necessary for execution of clinical trials and reinforcement of the company’s brand
• Ensure that staff achieve expected quality compliance standards
• Support staff to achieve delivery of study objectives
• Provide leadership in the continuous improvement in performance
• Support staff with action plan development and resolution of findings from Clinical Quality Assurance audits
• Conduct resource planning and metrics review with site management
• Conduct staff regular performance assessments and personal/career discussions with direct reports
• Responsible for providing regular updates to Director level Management and adhering to metrics
Education & Experience
• Profound knowledge of clinical trial processes and operations in Germany
• Familiar with ICH/GCP guidelines
• Several years of strong experience as a Project- and/or Program Manager
• Attention to detail, organizational skills, time management & prioritization
• Strong personality with great leadership and people skills
• Relationship management & influencing skills as well as presentation skills
• Proficiency in English and German
What is offered:
• 100% home based
• Interesting trials in various therapeutic areas.
• Unlimited employment contract with ICON
• Contribution to pension scheme
• Working exclusively with one client
• Position responsibility is planned to be extended to additional countries
Why this vacancy is right for you:
We offer an exciting and challenging work environment for clinical research professionals looking for an opportunity to contribute to the success of a company dedicated to researching, developing, manufacturing and marketing pharmaceuticals that improve health and quality of life.
Interested? Please submit your CV to nadine.rabenstein@docsglobal.com. We are looking forward to getting to know you.