Redbock: Specialized Life Sciences Consulting
Redbock, an NES Fircroft company, stands as a premier consultancy delivering customized resourcing solutions to pharmaceutical, biotechnology, medical device, and diagnostics companies. Founded in 2010 and headquartered in Encinitas, California, this privately-held firm has built a reputation for connecting resource-challenged organizations with highly skilled consultants who drive meaningful impact in the life sciences industry.
Excellence Through Expertise and Collaboration
As part of the award-winning NES Fircroft workforce specialist network, Redbock combines boutique-level personalized service with global resources spanning Life Sciences, Energy, Construction & Infrastructure, Manufacturing, Chemicals, Mining, and IT sectors. With 51-200 dedicated professionals and a 4.4-star Glassdoor rating, the company's consultants have successfully delivered solutions to some of the industry's largest and most high-profile companies, demonstrating deep expertise in pharmaceutical manufacturing, regulatory compliance, biostatistics, and equipment validation.
Your Career At Redbock
Redbock offers consultants meaningful opportunities to:
- Work on cutting-edge pharmaceutical and biotechnology projects
- Collaborate with cross-functional teams on complex technical challenges
- Develop expertise in regulatory submissions and compliance
- Contribute to life-changing treatments and medical technologies
- Build careers with exposure to diverse industry challenges
- Access professional development through NES Fircroft's global network
- Enjoy flexible work arrangements, including remote opportunities with core working hour flexibility
Culture and Values
Redbock's approach centers on creating positive impact for both clients and consultants. The company values technical excellence, hands-on problem-solving, strong communication, and making a tangible difference in healthcare outcomes. Working here means joining a team that emphasizes expertise, relationship-building, and innovative solutions in manufacturing environments. Consultants benefit from a supportive culture that recognizes the importance of clear communication, analytical rigor, and collaborative problem-solving-essential qualities for navigating complex pharmaceutical challenges.
Why Choose Redbock
Beyond competitive compensation, Redbock consultants gain access to a thriving California biotechnology ecosystem, meaningful work contributing to healthcare innovation, and career development opportunities within the broader NES Fircroft network. The company's commitment to positively impacting consultants' lives reflects in its supportive work environment and focus on long-term professional growth.
Mission
Deliver customized resourcing solutions that connect skilled consultants with pharmaceutical and life sciences companies, creating positive impact for both clients and professionals.
Frequently Asked Questions
Jobs for Redbock - an NES Fircroft company in United States
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Redbock - an NES Fircroft company02298 Boston, MA
Redbock - an NES Fircroft company02298 Boston, MA
Redbock - an NES Fircroft company92189 San Diego, CA

Sr. Statistical Programmer
Description
Position Summary
Our client is seeking a highly skilled Senior Statistical Programmer to join their team on a long-term contract basis. This is a hands-on role ideal for someone with experience in a small sponsor or biotech environment, where close collaboration with cross-functional teams is key. This position requires strong experience with Phase III studies, BLA submissions, and SAS Macro development.
The role will also focus on quality control (QC) of vendor-delivered programming outputs, with some in-house programming to validate and compare analysis datasets.
Key Responsibilities
- Perform QC and validation of vendor-delivered analysis datasets, tables, listings, and figures (TLFs).
- Develop and maintaining SAS macros to support analysis datasets (SDTM/ADaM), TFLs, and regulatory (BLA) submissions
- Conduct limited in-house programming, primarily ADaM dataset development, to ensure vendor quality and compliance.
- Collaborate closely with internal Biostatistics, Data Management, and Clinical teams to support ongoing clinical studies.
- Ensure adherence to CDISC standards (ADaM and SDTM) and company programming best practices.
- Participate in cross-functional discussions to resolve data or analysis-related issues and ensure timely delivery of submission-ready outputs.
Qualifications
- 8-10+ years of hands-on statistical programming experience, preferably with a small biotech or pharma company
- Proven programming experience supporting Phase III clinical trials and BLA (Biologics License Application) submissions
- Must have advanced SAS macro development skills - experience developing and maintaining SAS macros to support analysis datasets (SDTM/ADaM), TFLs, and regulatory submissions
- Strong working knowledge of CDISC ADaM and SDTM standards, as well as TLF programming.
- Experience in Dermatology therapeutic area preferred.
- Excellent communication skills and demonstrated ability to work cross-functionally in a fast-paced, collaborative environment.

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