21 час назад
Clinical Development Director, Early Development – Cardiometabolic/General Medicine
274 789 - 371 773$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Development Director, Early Development – Cardiometabolic/General Medicine (Clinical Drug Development): Leading early-phase development of cardiometabolic and general medicine compounds from first-in-human studies through proof-of-concept with an accent on clinical strategy, trial design, and interpretation of safety, efficacy, pharmacodynamic, and pharmacokinetic data. Focus on developing protocols and regulatory submissions, evaluating biomarkers, collaborating across research and development functions, and providing strategic guidance to early development teams.
Location: United States — Remote
Salary: USD 274,788.85–371,773.15 annually
Company
is a biotechnology company developing medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.
What you will do
- Lead early-phase clinical development of cardiometabolic and general medicine compounds from first-in-human studies through proof-of-concept.
- Design and implement clinical development strategies, plans, protocols, informed consents, Investigator Brochures, and regulatory submissions.
- Review safety, efficacy, pharmacodynamic, and pharmacokinetic data from clinical studies.
- Develop and apply clinical biomarker strategies to support drug development.
- Collaborate with Precision Medicine, Research, Late Development, Regulatory, Safety, and Commercial colleagues.
- Evaluate external licensing and partnering opportunities and provide biomedical guidance to early development teams.
Requirements
- MD or DO degree from an accredited medical school.
- At least 2 years of industry, academic, basic science, or clinical research experience.
- Understanding of cardiometabolic and general medicine pathophysiology.
- Experience with clinical trial methodology, trial design, monitoring, implementation, and interpretation of results.
- Leadership, collaboration, decision-making, interpersonal, and presentation skills.
- Ability to work effectively in a matrix environment and collaborate with internal and external stakeholders.
Nice to have
- Board certification or eligibility in Internal Medicine, Cardiology, or Endocrinology.
- Residency training in Internal Medicine and a relevant subspecialty.
- At least 3 years of pharmaceutical or academic drug development experience, preferably in early-stage clinical trials.
- Publication track record and experience collaborating with pharmaceutical sponsors.
Culture & Benefits
- Collaborative, innovative, and science-based work environment.
- Health, dental, vision, life, disability, and flexible spending benefits for eligible employees and dependents.
- Retirement and savings plan with company contributions.
- Discretionary annual bonus and stock-based long-term incentives.
- Award-winning time-off plans and career development opportunities.
Hiring process
- Applications are accepted until a sufficient number of candidates is received or a candidate is selected.
- Sponsorship for the role is not guaranteed.
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