Director/Sr. Director of Clinical Development
- Employer
- Yoh, a Day & Zimmermann Company
- Location
- working from home
- Start date
- Jul 2, 2021
View more
- Discipline
- Clinical, Clinical Medicine, Clinical Research, Clinical Trials, Medical Affairs
- Required Education
- Doctorate/PHD/MD
- Position Type
- Full time
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Yoh has an exciting opportunity for a Director/Sr. Director of Clinical Development to join our rapidly growing client based in New York, NY. This full time, direct hire, remote opportunity is ideal for candidates with a background in Internal Medicine working across multi therapeutic areas.
Responsibilities:
Clinical study planning and execution
- Development of protocol concepts, protocols and clinical development plans for Company assets and for biotech clients
- Medical leadership in the execution of clinical trials - risk assessment, operational considerations, safety and efficacy considerations
- Medical monitoring and oversight of phase 2-4 trials
- Provide clinical trial design consulting services to biotech clients
Business development
- Review of potential client pipelines to develop scientific and data-driven commercial strategies
- Direct participation in introductory client calls and bid defenses
- Help identify potential opportunities based on client pipelines/scientific advances
Operational excellence
- Drive/contribute to trial operations and medical processes to achieve continued innovation and improvement
- Support the training and engagement of our Investigator network
Corporate strategy
- Based on review of the scientific landscape contribute to therapeutic areas strategy
- Based on the clinical trial design landscape contribute to study design and planning strategy
Training
- Clinical training for internal stakeholders and clinical trial sites (e.g. overviews of specific disease areas, drug mechanisms of action, protocol requirements, etc.
Patient recruitment
- Input into patient recruitment tools
- Ideas for recruitment strategies - i .e. creative ideas for where we can find patients
Key Qualifications
- At l east 5 years experience i n biotech (preferred), pharma or CRO to include protocol development and medical oversight/monitoring of phase 2-4 studies
- MD/DO degree required
- Board certified by accredited specialty board - Internal Medicine preferred
- Excellent written and verbal communication skills
- Strong analytical skills
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