First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Permanent

Discipline: Statistics

Location: United States

Associate Director, Biostatistics - Permanent - Bay Area, CA

Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science.

Proclinical is seeking an Associate Director, Biostatistics to join one of the most exciting Biotech's in the Bay Area.

The company already have successful Regulatory approvals and an extensive pipeline which is continuously progressing and growing where they are now keen to capitalize on by growing several business critical functions.

Primary Responsibilities:

The successful candidate will be responsible for leading the execution of statistical components of Development programs. This position will manage external statisticians and statistical programmers.

Skills & Requirements:

D. in Statistics, Biostatistics, or Mathematics
7+ years of experience in clinical trial development
Demonstrated ability for project management of projects in clinical development
Experience managing delivery of statistical projects by CROs

The Associate Director's responsibilities will be:

Work alongside Clinical Development, Regulatory, Manufacturing, and Commercial organizations on the design and execution of clinical trials in the portfolio.
Oversee execution of the statistical components of clinical studies by CROs and independent contractors.
Manage on-time and quality delivery of CRO-generated analyses results.
Partner with Statistical Programming in generation of statistical analyses for internal and external presentations, and validation statistical analyses results generated by CROs.
Partner with Statistical Programming in the evaluation of CDISC electronic data packages for completeness, regulatory standards compliance, and submission readiness.
Consult internal audit team in assessing regulatory compliance of CROs with respect to statistical SOPs.
Participate in standards governance and development of Biostatistical SOPs.

Compensation:

$200,000 to $220,000 per annum.

If you are having difficulty in applying or if you have any questions, please contact George Breen at g.breen@proclinical.com

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy

Related jobs

Senior Manager, Data Management

Salary

US$160000 - US$190000 per annum

Location:

San Francisco, USA

Step into the future of biotechnology, where your ideas can transform healthcare and change lives. Join a dedicated company that's driving scientific breakthroughs every day.