Associate Director, Clinical Science Liaison
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Job Location:
Monthly Salary:
Posted on:
14 hours ago
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Position Overview
The Associate Director Clinical Science Liaison provides clinical development expertise into a multi-disciplinary team engaged in advising clients internal stakeholders and interacting with sites and investigators in early through late-stage development of medical products. This role will provide clinical science liaison support as a member of core study teams responsible for establishingrelationships withKOLs/PIs to provide enhanced peer-to-peer clinical/medialsupport enabling prioritization of trial recruitment and quality trialdelivery and addressing scientifictrial queries. The role will also support the PPD clinical trial proposal process to provide trial design considerations and operational enhancement of trial execution.
Duties and Responsibilities
Strong teamwork skills required to work with a cross-functional consulting team (e.g. experts in clinical development strategy clinical research regulatory strategy CMC and toxicology strategy biostatistics clinical pharmacology and pharmacokinetics). In addition this role will be involved in projects in partnership with clinical trials teams who will provide additional training and guidance. Responsibilities including:
- Clinical science liaison activities including supporting KOLs PIs and clinical trial sites by actively engaging with site personnel overcoming recruitment challenges and concerns.
- Contribute to clinical trial scientific deliverables by providing scientific review and input to keystudy documents ensuring scientific rigor consistency and alignment with strategy.
- KOL mapping and coordination of key opinion leader advisory boards
- Contribute to clinical trial feasibility outreach through P2P discussions
- Support Clinical Development Leads with competitive intelligence for clinical development plans and strategic program assessments regulatory submissions and trial design.
Education and Experience
- MD PhD PharmD or equivalent in a scientific discipline or related field required
- Expertise and experience with the conduct of global clinical trials for medical products clinical training and/or experience strongly preferred
- Seeking an experienced professional with exceptional client and site personnel facing skills.
- Familiarity with various clinical trial designs including more complex trials study outcome interpretation skills
- 6 years of experience (following receipt of doctoral degree) in a clinical research setting such as biotech/pharmaceutical industry academia government and/or non-profit.
- Experience in Respiratory Medicine Neuroscience/Ophthalmology or Immunology/Rheumatology/Inflammation with the ability to cross-cover in additional therapeutic areas is strongly preferred
- Expert in navigating scientific literature interpretation of data and display of data
- Knowledge of GCP/IHC regulatory guidelines and precedents
- Excellent interpersonal and communication skills. Strong attention to detail. Good organizational prioritization and time management skills.
- Ability to work on multiple projects simultaneously
- Ability to work both independently and in a team environment
- Highly proficient in standard computer software (MS Word Excel PowerPoint) Clinical Trial Databases Clinical Trial Intelligence Tools.
- Ability to speak multiple languages preferred
Required Experience:
Director
Key Skills
- Presentation Skills
- Time Management
- Clinical Research
- Communication skills
- GCP
- Infusion Experience
- Managed Care
- Hospice Care
- Conflict Management
- Clinical Trials
- Research Experience
- Home Care
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
