Senior Medical Director, Clinical Development Ophthalmology
- $300,000 - $350,000
- Palo Alto, CA
NEW Senior Medical Director Clinical Development opportunity!
A bit about us:
We are a clinical stage biopharmaceutical focused in multiple therapeutic areas, including ophthalmology, and looking to grow the team with a Senior Medical Director-VP level Clinical Development! Please contact me for further details.
Why join us?
Competitive benefits package
Opportunity for growth
Flexible schedule
Strong pipeline
Opportunity for growth
Flexible schedule
Strong pipeline
Job Details
Job Details
We are seeking a dynamic and experienced individual to join our team as a full time Senior Medical Director, Clinical Development. This role is a unique opportunity to make a significant impact in a fast-paced, innovative, and growing scientific industry. You will be responsible for leading clinical development activities for our pipeline of novel therapeutics. This is a strategic role that will require you to work closely with cross-functional teams, including research, regulatory, and commercial teams, to ensure the successful development of our innovative products.
Responsibilities
As a Senior Medical Director, Clinical Development, you will:
1. Lead the design, execution, and interpretation of clinical trials for our pipeline products, ensuring all activities are compliant with GCP guidelines.
2. Develop and implement clinical development strategies for early and late-stage drug development programs, with a focus on rare diseases and ophthalmology.
3. Oversee the preparation of clinical protocols, investigator brochures, IND, and NDA submissions, ensuring all documents are scientifically sound and meet regulatory requirements.
4. Collaborate with cross-functional teams to ensure alignment of clinical development strategies with business objectives.
5. Provide medical and scientific expertise to internal teams, advisory boards, and key opinion leaders.
6. Monitor and interpret data from ongoing and completed studies, and recommend modifications to future studies as necessary.
7. Stay current with latest developments in biotechnology and clinical research, and adapt strategies as needed.
Qualifications
The ideal candidate will have:
1. A medical degree with a specialty in ophthalmology or a related field.
2. A minimum of 12 years of experience in clinical development in the biotechnology or pharmaceutical space/.
3. Proven experience in designing and managing clinical trials, including early and late-stage drug development.
4. Strong knowledge of GCP, IND, and NDA requirements, and experience in preparing regulatory documents.
5. Experience in rare disease drug development and ophthalmology is highly desirable.
6. Strong leadership skills, with the ability to influence and work effectively with cross-functional teams.
7. Excellent analytical, problem-solving, and decision-making skills.
8. Outstanding communication and presentation skills, with the ability to clearly convey complex scientific information to a variety of audiences.
We are looking for a driven and passionate individual who is ready to contribute to our mission of advancing innovative therapies for patients. If you are looking to make a significant impact in a fast-paced, innovative environment, we would love to hear from you.
We are seeking a dynamic and experienced individual to join our team as a full time Senior Medical Director, Clinical Development. This role is a unique opportunity to make a significant impact in a fast-paced, innovative, and growing scientific industry. You will be responsible for leading clinical development activities for our pipeline of novel therapeutics. This is a strategic role that will require you to work closely with cross-functional teams, including research, regulatory, and commercial teams, to ensure the successful development of our innovative products.
Responsibilities
As a Senior Medical Director, Clinical Development, you will:
1. Lead the design, execution, and interpretation of clinical trials for our pipeline products, ensuring all activities are compliant with GCP guidelines.
2. Develop and implement clinical development strategies for early and late-stage drug development programs, with a focus on rare diseases and ophthalmology.
3. Oversee the preparation of clinical protocols, investigator brochures, IND, and NDA submissions, ensuring all documents are scientifically sound and meet regulatory requirements.
4. Collaborate with cross-functional teams to ensure alignment of clinical development strategies with business objectives.
5. Provide medical and scientific expertise to internal teams, advisory boards, and key opinion leaders.
6. Monitor and interpret data from ongoing and completed studies, and recommend modifications to future studies as necessary.
7. Stay current with latest developments in biotechnology and clinical research, and adapt strategies as needed.
Qualifications
The ideal candidate will have:
1. A medical degree with a specialty in ophthalmology or a related field.
2. A minimum of 12 years of experience in clinical development in the biotechnology or pharmaceutical space/.
3. Proven experience in designing and managing clinical trials, including early and late-stage drug development.
4. Strong knowledge of GCP, IND, and NDA requirements, and experience in preparing regulatory documents.
5. Experience in rare disease drug development and ophthalmology is highly desirable.
6. Strong leadership skills, with the ability to influence and work effectively with cross-functional teams.
7. Excellent analytical, problem-solving, and decision-making skills.
8. Outstanding communication and presentation skills, with the ability to clearly convey complex scientific information to a variety of audiences.
We are looking for a driven and passionate individual who is ready to contribute to our mission of advancing innovative therapies for patients. If you are looking to make a significant impact in a fast-paced, innovative environment, we would love to hear from you.
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Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.
Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policy