3 months ago

Associate Director, Clinical Science

✓ Verified Job

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

Source: Company careers pageValidated by: Fursa AI

Last checked: 55 minutes agoStatus: Live

Job Summary

Lead and shape oncologic clinical development programs by coordinating cross-functional teams, external vendors, and investigators to ensure timely, compliant execution of trials; oversee data review, protocol development, and study execution timelines while building relationships with KOLs and sites to support regulatory submissions.

Location: United States

Workplace: Remote

Employment Type: Full time

Job Function: Executive & General Management

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

Pay and Benefits

Perks:Health InsuranceDentalVision401kCommuter Benefits

Key Requirements

•Advanced degree in Life Sciences (MD, PhD, Pharm D, MS, RN or similar scientific field) preferred
•8+ years 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:8+ yearsOncologyClinical developmentPharma/biotechClinical trialsMolecular diagnostics

Education:PhD / Doctorate

Skills:CommunicationLeadershipProblem-solvingOrganizationalAnalytical

Languages:English

Tech Stack:GoogleMicrosoft 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

Associate Director, Clinical Science

✓ Verified Job

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

Source: Company careers pageValidated by: Fursa AI

Last checked: 55 minutes agoStatus: Live

Job Summary

Location: United States

Workplace: Remote

Employment Type: Full time

Job Function: Executive & General Management

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

Pay and Benefits

Perks:Health InsuranceDentalVision401kCommuter Benefits

Key Requirements

•Advanced degree in Life Sciences (MD, PhD, Pharm D, MS, RN or similar scientific field) preferred
•8+ years 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:8+ yearsOncologyClinical developmentPharma/biotechClinical trialsMolecular diagnostics

Education:PhD / Doctorate

Skills:CommunicationLeadershipProblem-solvingOrganizationalAnalytical

Languages:English

Tech Stack:GoogleMicrosoft 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