21 час назад
Scientific Director II, Oncology Early Development
182 000 - 346 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Scientific Director II, Oncology Early Development (Clinical Development/Oncology): Leads the design, implementation, analysis, and reporting of clinical development programs and trials supporting oncology medicines with an accent on scientific strategy, regulatory compliance, and cross-functional collaboration. Focus on interpreting safety and efficacy data, developing protocols and regulatory submissions, overseeing study integrity and timelines, and guiding translational and clinical development activities.
Location: Florham Park, New Jersey, United States
Salary: $182,000–$346,000 per year
Company
Biopharmaceutical organization focused on discovering and delivering medicines and solutions for serious health issues, including oncology.
What you will do
- Lead the design and implementation of multiple clinical development programs or one large, complex program.
- Direct clinical study teams, monitor study integrity, and interpret and communicate accumulating safety and efficacy data.
- Own the scientific content of protocols, Investigator Brochures, clinical study reports, regulatory submissions, and responses.
- Develop cross-functional Clinical Development Plans and contribute to Integrated Evidence Strategy Teams and Asset Development Teams.
- Coordinate scientific and medical activities for oncology molecules and diseases with internal stakeholders and external opinion leaders.
- Support translational strategies, business development diligence, regulatory discussions, and adherence to Good Clinical Practices and pharmacovigilance standards.
Requirements
- Bachelor's degree in a scientific discipline; an MS, PhD, or PharmD is preferred.
- At least 5 years of clinical trial experience in the pharmaceutical industry, academia, or an equivalent setting.
- Experience with clinical trial methodology, regulatory and compliance requirements, clinical strategy, and study protocol design.
- Ability to oversee moderately complex clinical research programs with minimal supervision.
- Ability to provide direction, collaborate across global cross-functional teams, and support scientific and business strategy.
- Excellent written and spoken English communication skills are required.
Culture & Benefits
- Paid vacation, holidays, and sick leave.
- Medical, dental, and vision insurance for eligible employees.
- 401(k) benefits for eligible employees.
- Eligibility to participate in long-term incentive programs.
- Equal opportunity employment and a workplace committed to integrity, innovation, and community service.
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