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Associate Director, Study Site Engagement(m/w/x)
Developing site engagement strategies for clinical trials in GI, oncology, and rare diseases at a biotech firm for life-changing therapies. Scientific degree and 10+ years clinical research experience required. Global collaboration across diverse study teams and CROs.
Requirements
- Scientific degree in pharmaceutical science, chemistry, biology, or healthcare
- 10+ years of experience in clinical research
- Ability to work independently and in teams
- Global cross-functional collaboration skills
- Global and cross boundary communication skills
- Business acumen
- Organization and planning skills
- Time management skills
- Emotional intelligence
- Problem solving skills
- Relationship management and influencing skills
- Fluency in spoken and written English
- Flexibility
- Decision making skills
Tasks
- Partner with study teams and CROs
- Establish regional Medical Affairs communication
- Develop study-specific site engagement strategies
- Support trial operations from feasibility to CSR
- Identify and select potential study sites
- Nurture long-term relationships with investigators
- Mitigate recruitment barriers for clinical programs
- Track feasibility progress and escalate issues
- Liaise with local Clinical Operations teams
- Attend pre-study and site initiation visits
- Resolve start-up hurdles to ensure activations
- Coordinate recruitment activities and booster visits
- Interact regularly with priority trial sites
- Manage regional SSE talent and resources
- Represent the company at clinical conferences
- Maintain strategic relationships with site networks
Work Experience
- 10 years
Education
- Master's degree
Languages
- English – Business Fluent
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Associate Director, Study Site Engagement(m/w/x)
Developing site engagement strategies for clinical trials in GI, oncology, and rare diseases at a biotech firm for life-changing therapies. Scientific degree and 10+ years clinical research experience required. Global collaboration across diverse study teams and CROs.
Requirements
- Scientific degree in pharmaceutical science, chemistry, biology, or healthcare
- 10+ years of experience in clinical research
- Ability to work independently and in teams
- Global cross-functional collaboration skills
- Global and cross boundary communication skills
- Business acumen
- Organization and planning skills
- Time management skills
- Emotional intelligence
- Problem solving skills
- Relationship management and influencing skills
- Fluency in spoken and written English
- Flexibility
- Decision making skills
Tasks
- Partner with study teams and CROs
- Establish regional Medical Affairs communication
- Develop study-specific site engagement strategies
- Support trial operations from feasibility to CSR
- Identify and select potential study sites
- Nurture long-term relationships with investigators
- Mitigate recruitment barriers for clinical programs
- Track feasibility progress and escalate issues
- Liaise with local Clinical Operations teams
- Attend pre-study and site initiation visits
- Resolve start-up hurdles to ensure activations
- Coordinate recruitment activities and booster visits
- Interact regularly with priority trial sites
- Manage regional SSE talent and resources
- Represent the company at clinical conferences
- Maintain strategic relationships with site networks
Work Experience
- 10 years
Education
- Master's degree
Languages
- English – Business Fluent
About the Company
Takeda
Industry
Pharmaceuticals
Description
Das Unternehmen fokussiert sich darauf, lebensverändernde Therapien in den Bereichen Magen-Darm- und Entzündungskrankheiten, seltene Krankheiten, Onkologie, Neurowissenschaften und Impfstoffe zu entdecken und bereitzustellen.
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- BeOne Medicines Germany GmbH
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Dedicated Line Manager of Clinical Project Managers(m/w/x)
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Clinical Associate Submissions – Regulatory(m/w/x)
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