Director of Statistical Programming
Scientific Search, Princeton, NJ, United States
Director, Statistical Programming | Oncology Biotech (Late-Stage)
Location: Remote (East Coast Preferred)
Reports into Sr. Director – Head of Biostats
Salary: $210‑225k base (flexible to go higher for the right individual).
We’re partnering with a
100+ person oncology company
entering a critical phase of growth, with multiple programs advancing toward global submissions. This is a
high‑visibility leadership role
where you’ll shape programming strategy across pivotal studies and regulatory filings.
If you’ve led
ISS/ISE, global submissions, and high-performing programming teams , this is the kind of role where you can truly influence outcomes.
Why This Role Stands Out
Own programming strategy across late-stage oncology programs
Lead global submissions (NDA/BLA/MAA) and integrated analyses
Drive innovation using R, Python, and modern data platforms
Partner directly with Biostatistics, Clinical, and executive stakeholders
Build and scale processes in a growing, fast-moving biotech environment
What you’ll be doing
Leading integrated safety and efficacy analyses (ISS/ISE) at the program level
Overseeing global programming operations and vendor partnerships
Driving submission readiness including TLFs, define.xml, and reviewers’ guides
Establishing scalable, audit-ready programming standards and SOPs
Acting as a senior leader across cross‑functional clinical teams
What they’re looking for
15–18+ years in pharma/CRO with deep experience in oncology programming
Proven leadership in global submissions and integrated analyses
Strong expertise in SAS, CDISC (SDTM/ADaM), and regulatory standards
Track record leading global teams and managing external vendors
This is an opportunity to step into a
strategic leadership role
at a company where your work will directly impact regulatory success and patient outcomes.
Message me directly or email tom@scientificsearch.com to learn more.
#J-18808-Ljbffr
Location: Remote (East Coast Preferred)
Reports into Sr. Director – Head of Biostats
Salary: $210‑225k base (flexible to go higher for the right individual).
We’re partnering with a
100+ person oncology company
entering a critical phase of growth, with multiple programs advancing toward global submissions. This is a
high‑visibility leadership role
where you’ll shape programming strategy across pivotal studies and regulatory filings.
If you’ve led
ISS/ISE, global submissions, and high-performing programming teams , this is the kind of role where you can truly influence outcomes.
Why This Role Stands Out
Own programming strategy across late-stage oncology programs
Lead global submissions (NDA/BLA/MAA) and integrated analyses
Drive innovation using R, Python, and modern data platforms
Partner directly with Biostatistics, Clinical, and executive stakeholders
Build and scale processes in a growing, fast-moving biotech environment
What you’ll be doing
Leading integrated safety and efficacy analyses (ISS/ISE) at the program level
Overseeing global programming operations and vendor partnerships
Driving submission readiness including TLFs, define.xml, and reviewers’ guides
Establishing scalable, audit-ready programming standards and SOPs
Acting as a senior leader across cross‑functional clinical teams
What they’re looking for
15–18+ years in pharma/CRO with deep experience in oncology programming
Proven leadership in global submissions and integrated analyses
Strong expertise in SAS, CDISC (SDTM/ADaM), and regulatory standards
Track record leading global teams and managing external vendors
This is an opportunity to step into a
strategic leadership role
at a company where your work will directly impact regulatory success and patient outcomes.
Message me directly or email tom@scientificsearch.com to learn more.
#J-18808-Ljbffr