3 months ago

Director, Clinical Science

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 56 minutes agoStatus: Live

Job Summary

Lead and oversee clinical science for oncology programs, developing study concepts, protocols, and data review plans. Collaborate cross-functionally with clinical development, operations, regulatory, biostatistics, and translational medicine to ensure timely, compliant program execution. Manage CROs, provide training, and mentor junior scientists while maintaining strong relationships with investigators and KOLs. Travel up to 25% as needed in a fast-paced, global environment.

Location: United States

Workplace: Remote

Employment Type: Full time

Job Function: Executive & General Management

Seniority: Director level

Key Responsibilities

•Develop study concepts, including study design, schedule of assessments, objectives/endpoints, and eligibility criteria
•Collaborate cross-functionally to develop Protocol and ICF documents / amendments and present these to governance committee and early clinical development team meetings as required
•Provide protocol training and contribute to CRF design
•Ensure study manuals align with protocol and engage investigators in study design
•Seek input from key investigators on study design and methodology to ensure alignment with research objectives, and actively participate in pre-site selection discussions, site initiation visits, and investigator meetings to support successful study execution

Travel: Low travel

Pay and Benefits

Salary: USD 192,600 - 240,800 annually

Perks:Health InsuranceDentalVisionLife InsuranceDisability401kCommuter BenefitsReferral ProgramFertility Care

Key Requirements

•Advanced degree in Life Sciences (MD, PhD, Pharm D, MS, RN or similar scientific field) preferred
•10+ years of pharma/biotech industry experience in clinical development in oncology clinical trials
•Deep understanding and preferably experience in oncology molecular diagnostics, oncology companion diagnostics or early cancer detection
•Experience in data review, data cleaning, managing and interpreting clinical trials results as well in writing clinical trial protocols
•Possesses sound foundational knowledge of FDA and other major country regulations and detailed knowledge of Good Clinical Practice other regulations governing clinical research

Experience:10+ yearsOncologyBiotechClinical developmentPharmaClinical trials

Education:Professional (JD, MD, etc.) in Life Sciences

Skills:LeadershipCommunicationProblem-solvingAttention to detailCross-functional collaboration

Languages:English

Tech Stack:Google SuiteMicrosoft Office

Company Brief

Natera

Develops and commercializes genetic testing and diagnostics focused on reproductive health, oncology, and organ transplant to inform clinical decision-making and improve patient outcomes.

Industry: Diagnostics

Company Size: Enterprise (1,001+ employees)

Revenue: USD 500M to 1B

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: San Carlos, United States

Founded: 2004

Website LinkedIn

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Natera

3 months ago

Director, Clinical Science

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 56 minutes agoStatus: Live

Job Summary

Location: United States

Workplace: Remote

Employment Type: Full time

Job Function: Executive & General Management

Seniority: Director level

Key Responsibilities

•Develop study concepts, including study design, schedule of assessments, objectives/endpoints, and eligibility criteria
•Collaborate cross-functionally to develop Protocol and ICF documents / amendments and present these to governance committee and early clinical development team meetings as required
•Provide protocol training and contribute to CRF design
•Ensure study manuals align with protocol and engage investigators in study design
•Seek input from key investigators on study design and methodology to ensure alignment with research objectives, and actively participate in pre-site selection discussions, site initiation visits, and investigator meetings to support successful study execution

Travel: Low travel

Pay and Benefits

Salary: USD 192,600 - 240,800 annually

Perks:Health InsuranceDentalVisionLife InsuranceDisability401kCommuter BenefitsReferral ProgramFertility Care

Key Requirements

•Advanced degree in Life Sciences (MD, PhD, Pharm D, MS, RN or similar scientific field) preferred
•10+ years of pharma/biotech industry experience in clinical development in oncology clinical trials
•Deep understanding and preferably experience in oncology molecular diagnostics, oncology companion diagnostics or early cancer detection
•Experience in data review, data cleaning, managing and interpreting clinical trials results as well in writing clinical trial protocols
•Possesses sound foundational knowledge of FDA and other major country regulations and detailed knowledge of Good Clinical Practice other regulations governing clinical research

Experience:10+ yearsOncologyBiotechClinical developmentPharmaClinical trials

Education:Professional (JD, MD, etc.) in Life Sciences

Skills:LeadershipCommunicationProblem-solvingAttention to detailCross-functional collaboration

Languages:English

Tech Stack:Google SuiteMicrosoft Office

Company Brief

Natera

Develops and commercializes genetic testing and diagnostics focused on reproductive health, oncology, and organ transplant to inform clinical decision-making and improve patient outcomes.

Industry: Diagnostics

Company Size: Enterprise (1,001+ employees)

Revenue: USD 500M to 1B

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: San Carlos, United States

Founded: 2004

Website LinkedIn