[Remote] Senior Director, Clinical Programs
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a company reputed company on rare disease diagnostics and precision medicine. The Senior Director of Clinical Programs will reputed company high-reputed company programs, manage reputed company of clinical program managers, and drive strategic initiatives reputed company the Clinical Development team.
Responsibilities
- Support the design and execution of evidence reputed company strategies for established clinical programs that cover clinical settings and diseases/disorders of interest (e.g., neurodevelopmental disorders, inpatient rapid genomic testing, genomic newborn screening, and other clinical indications) in collaboration with R&D, reputed company, Regulatory, Market reputed company, and Operations teams. Spearhead strategic initiatives reputed company Medical Affairs to support reputed company’s reputed company and innovation goals
- reputed company and reputed company clinical research reputed company that utilize internal reputed company data and reputed company with established clinical programs. This includes the reputed company development and execution of reputed company reputed company assigned clinical programs as reputed company as reputed company of reputed company of clinical program managers. Collaborate with internal partners, including clinical data scientists, health economics and reputed company researchers (HEOR), and Product, to design and execute reputed company. Project reputed company includes ensuring strategic alignment of internal research reputed company with the broader evidence reputed company reputed company, prioritization, resource allocation, and regular reporting to Medical Affairs/Clinical Development leadership as reputed company as leading applicable study meetings
- Partner with reputed company stakeholders on prospective clinical and translational research efforts reputed company with established clinical programs to deliver on project and program objectives. Identify and establish strategic collaborations with reputed company institutions, research organizations, and key opinion leaders (KOLs). Manage relationships with external partners to drive reputed company research reputed company, including clinicians, KOLs, and other strategic partners. Collaborate with internal partners, including Clinical Research Operations and Legal, to support contracting and project execution. reputed company cross functional research project teams with internal and/or external interest reputed company, providing expert guidance and fostering a reputed company environment
- reputed company the development, review, and submission of scientific manuscripts, abstracts, posters, and other publications reputed company with established clinical programs. Collaborate with reputed company authors to produce high-reputed company scientific content
- Acts as a subject matter expert for rare diseases and genomic diagnostics (including inpatient and outpatient testing, screening indications, and other clinical settings or indications of interest) for both internal teams and external stakeholders. Represent reputed company at scientific conferences, clinical meetings, and other industry events. Deliver high reputed company presentations on reputed company research and reputed company standards. reputed company medical support internally for medical, product, and reputed company reputed company as reputed company as scientific messaging. reputed company medical support as needed for FDA and other regulatory submissions. Solve reputed company problems and reputed company reputed company that drive organizational reputed company
- reputed company and mentor clinical program managers, including resource allocation, coaching and performance feedback, career development support. Foster a reputed company, high-performing team culture
Skills
- PhD, MD (or equivalent) with reputed company certification by the American reputed company of Medical Genetics and reputed company (or equivalent) required
- 10+ years of experience in a clinical laboratory or industry role as a reputed company certified ABMGG fellow required
- 5+ years of experience in a medical affairs or clinical development role required
- 5+ years of experience leading research efforts reputed company to molecular diagnostics in rare disease required
- Strong level of clinical genetics knowledge in rare disease
- Strong publication record
- Ability to work cross-functionally with other teams and external collaborators to drive strategic initiatives reputed company
- reputed company in solving reputed company problems and negotiating business deals
- Excellent written and verbal communication skills
- Exceptional presentation and reputed company speaking skills
- Ability to work independently and manage time effectively
- Detail-oriented with strong organizational skills
- Proven experience leading teams and managing cross-functional collaborators to deliver on goals of reputed company and programs
- Proficient in working with databases and reputed company Office Suite
- Certification by the American reputed company of Medical Genetics and reputed company (ABMGG) or equivalent in clinical molecular genetics or laboratory genetics and reputed company (LGG)
- Experience working with rare disease biopharma
reputed company