Investigo
Director / Sr Director, Clinical Science (Oncology, Contract)
Investigo, San Francisco, California, United States, 94199
Director / Sr Director, Clinical Science (Oncology, Contract)
1 day ago Be among the first 25 applicants
This range is provided by Investigo. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $180.00/hr - $200.00/hr
Direct message the job poster from Investigo
Talent Consultant | Focused on Quality & Compliance We are supporting a
confidential, public, clinical-stage biotechnology company
focused on
precision oncology . The organization is advancing multiple targeted oncology programs and is seeking an experienced
Clinical Science leader
to support ongoing and upcoming clinical studies.
This role partners closely with senior oncology development leadership and serves as the
medical-scientific voice
on one or more clinical programs. The position is
hands‑on , execution‑focused, and ideal for someone who enjoys being deeply embedded in study design, data interpretation, and cross‑functional collaboration.
Key Responsibilities
Partner with clinical leadership to develop
clinical development concepts and plans , with emphasis on early oncology programs
Lead or contribute to
protocol synopses, protocols, and amendments
Author and review
informed consent forms (ICFs)
and adjudicate site‑specific ICF requests
Collaborate with
Clinical Operations
on site selection, start‑up, and ongoing site communication
Write and maintain
Investigator Brochures , including annual updates
Contribute to or author
clinical and safety sections
of regulatory submissions (e.g., NDA/MAA)
Represent Clinical Science on
cross‑functional study teams
Review and interpret
clinical data listings , including safety and SAE data
Author or support
Clinical Study Reports (CSRs)
and related publications
Develop study‑ and program‑level
presentations and slide decks
Train internal teams, CROs, and site staff on protocols and therapeutic area
Support
Health Authority interactions , including responses to inspections and audits
Assist with or serve as
Medical Monitor
for Phase 2 or Phase 3 clinical trials
Qualifications
Bachelor’s degree required with strong clinical oncology knowledge
Advanced degree preferred (MD, PharmD, PhD, NP, or Master’s in a relevant field)
4+ years of industry oncology clinical development experience
Demonstrated involvement across the
full clinical trial lifecycle
(start‑up through CSR)
Experience with
small‑molecule oncology trials
strongly preferred
Strong skills in
protocol design, data interpretation, and safety oversight
Working knowledge of
Good Clinical Practice (GCP)
Excellent written and verbal communication skills
Ability to thrive in a
fast‑paced, evolving biotech environment
Candidates from closely related disciplines (e.g., Clinical Operations, Regulatory Affairs, Biometrics) who have represented their function on study teams may also be considered.
Additional Information
On‑site presence is required
(San Diego or South San Francisco)
This is a 18‑month
contract position
with high visibility and impact
#J-18808-Ljbffr
This range is provided by Investigo. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $180.00/hr - $200.00/hr
Direct message the job poster from Investigo
Talent Consultant | Focused on Quality & Compliance We are supporting a
confidential, public, clinical-stage biotechnology company
focused on
precision oncology . The organization is advancing multiple targeted oncology programs and is seeking an experienced
Clinical Science leader
to support ongoing and upcoming clinical studies.
This role partners closely with senior oncology development leadership and serves as the
medical-scientific voice
on one or more clinical programs. The position is
hands‑on , execution‑focused, and ideal for someone who enjoys being deeply embedded in study design, data interpretation, and cross‑functional collaboration.
Key Responsibilities
Partner with clinical leadership to develop
clinical development concepts and plans , with emphasis on early oncology programs
Lead or contribute to
protocol synopses, protocols, and amendments
Author and review
informed consent forms (ICFs)
and adjudicate site‑specific ICF requests
Collaborate with
Clinical Operations
on site selection, start‑up, and ongoing site communication
Write and maintain
Investigator Brochures , including annual updates
Contribute to or author
clinical and safety sections
of regulatory submissions (e.g., NDA/MAA)
Represent Clinical Science on
cross‑functional study teams
Review and interpret
clinical data listings , including safety and SAE data
Author or support
Clinical Study Reports (CSRs)
and related publications
Develop study‑ and program‑level
presentations and slide decks
Train internal teams, CROs, and site staff on protocols and therapeutic area
Support
Health Authority interactions , including responses to inspections and audits
Assist with or serve as
Medical Monitor
for Phase 2 or Phase 3 clinical trials
Qualifications
Bachelor’s degree required with strong clinical oncology knowledge
Advanced degree preferred (MD, PharmD, PhD, NP, or Master’s in a relevant field)
4+ years of industry oncology clinical development experience
Demonstrated involvement across the
full clinical trial lifecycle
(start‑up through CSR)
Experience with
small‑molecule oncology trials
strongly preferred
Strong skills in
protocol design, data interpretation, and safety oversight
Working knowledge of
Good Clinical Practice (GCP)
Excellent written and verbal communication skills
Ability to thrive in a
fast‑paced, evolving biotech environment
Candidates from closely related disciplines (e.g., Clinical Operations, Regulatory Affairs, Biometrics) who have represented their function on study teams may also be considered.
Additional Information
On‑site presence is required
(San Diego or South San Francisco)
This is a 18‑month
contract position
with high visibility and impact
#J-18808-Ljbffr