Sr. Medical Director Clinical Development
- $250,000 - $315,000
- San Diego, CA
Sr. Oncology Medical Director Clinical Development Opportunity
A bit about us:
We are a biotech company hiring for a Sr. Medical Director in Clinical Development, with a background in oncology. Please apply to discuss further details!
Why join us?
Competitive compensation package
Opportunity for growth
Benefits
401k
Remote work
Opportunity for growth
Benefits
401k
Remote work
Job Details
Job Details:
We are seeking a dynamic, highly skilled, and passionate individual to join our team as a Permanent Sr. Medical Director of Clinical Development in the Scientific industry. This is a unique opportunity to contribute to the development of innovative therapies that can make a significant impact on patients' lives. The Sr. Medical Director will play a pivotal role in overseeing and leading the clinical strategy with a focus on safety, data, and medical aspects. The ideal candidate should have a strong understanding of KOLs and be able to communicate effectively with various stakeholders.
Responsibilities:
1. Lead the development and execution of clinical development strategies for assigned projects.
2. Oversee the safety and medical data review process to ensure the highest quality and integrity.
3. Establish and maintain relationships with Key Opinion Leaders (KOLs) in relevant therapeutic areas.
4. Provide medical and scientific expertise to cross-functional teams.
5. Ensure compliance with global regulatory and ethical standards for clinical trials.
6. Collaborate with internal and external partners to ensure successful execution of clinical trials.
7. Provide medical oversight and guidance to the clinical operations team.
8. Participate in the preparation and review of regulatory documents, clinical study reports, and other clinical documents.
9. Drive the interpretation, presentation, and dissemination of clinical trial data.
10. Stay abreast of the latest scientific and medical advancements in the relevant therapeutic areas.
Qualifications:
1. MD or equivalent with a minimum of 5 years of experience in clinical development in the pharmaceutical or biotech industry.
2. Strong knowledge of clinical research methodology, regulatory requirements, and medical terminology.
3. Proven experience in building and maintaining relationships with KOLs.
4. Strong analytical skills with the ability to interpret complex clinical data.
5. In-depth knowledge of safety and risk management.
6. Excellent leadership and team management skills.
7. Strong communication and presentation skills.
8. Ability to work effectively in a fast-paced, dynamic environment.
9. High ethical standards with a strong commitment to patient safety.
10. Willingness to travel as required.
Join us in this exciting role and contribute to the development of innovative therapies that can change patients' lives. We offer a competitive compensation package and an opportunity to work in a stimulating and collaborative environment.
We are seeking a dynamic, highly skilled, and passionate individual to join our team as a Permanent Sr. Medical Director of Clinical Development in the Scientific industry. This is a unique opportunity to contribute to the development of innovative therapies that can make a significant impact on patients' lives. The Sr. Medical Director will play a pivotal role in overseeing and leading the clinical strategy with a focus on safety, data, and medical aspects. The ideal candidate should have a strong understanding of KOLs and be able to communicate effectively with various stakeholders.
Responsibilities:
1. Lead the development and execution of clinical development strategies for assigned projects.
2. Oversee the safety and medical data review process to ensure the highest quality and integrity.
3. Establish and maintain relationships with Key Opinion Leaders (KOLs) in relevant therapeutic areas.
4. Provide medical and scientific expertise to cross-functional teams.
5. Ensure compliance with global regulatory and ethical standards for clinical trials.
6. Collaborate with internal and external partners to ensure successful execution of clinical trials.
7. Provide medical oversight and guidance to the clinical operations team.
8. Participate in the preparation and review of regulatory documents, clinical study reports, and other clinical documents.
9. Drive the interpretation, presentation, and dissemination of clinical trial data.
10. Stay abreast of the latest scientific and medical advancements in the relevant therapeutic areas.
Qualifications:
1. MD or equivalent with a minimum of 5 years of experience in clinical development in the pharmaceutical or biotech industry.
2. Strong knowledge of clinical research methodology, regulatory requirements, and medical terminology.
3. Proven experience in building and maintaining relationships with KOLs.
4. Strong analytical skills with the ability to interpret complex clinical data.
5. In-depth knowledge of safety and risk management.
6. Excellent leadership and team management skills.
7. Strong communication and presentation skills.
8. Ability to work effectively in a fast-paced, dynamic environment.
9. High ethical standards with a strong commitment to patient safety.
10. Willingness to travel as required.
Join us in this exciting role and contribute to the development of innovative therapies that can change patients' lives. We offer a competitive compensation package and an opportunity to work in a stimulating and collaborative environment.
Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
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.
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.