R&D Partners

About the Company

R&D Partners is a global functional service provider & strategic staffing resource specializing in scientific, clinical research & engineering. The cornerstone of our success starts with a knowledgeable and experienced team of life science professionals. After assessing our clients' project resourcing needs, our team can deliver the appropriate workforce solution focusing on the unique skills and experience your project requires.

Established in 2007, we partner with the world's leading biopharmaceutical, medical device, and diagnostic companies, focusing on their unique research & development resourcing needs. We pride ourselves as a niche life science provider partnered with the leading global healthcare & life science solutions provider Acacium Group.

Parent Company:
https://acaciumgroup.com/

Listed Jobs

Company Name

R&D Partners

Job Title

Consultant RWE Statistician (Home-Based, Europe)

Job Description

**Job Title**: Consultant RWE Statistician (Home‑Based, Europe) **Role Summary** Provide statistical expertise for Real‑World Evidence (RWE) and Health Economics & Outcomes Research (HEOR) studies. Manage end‑to‑end statistical activities, develop study and analysis plans, review and oversee vendor work, and implement innovative statistical methods to enhance study quality and integrity. **Expectations** - Remote/home‑based work - Ability to collaborate cross‑functionally with clinical, medical, and data science teams - Deliver high‑quality statistical analyses and reports within project timelines **Key Responsibilities** - Lead statistical analysis for RWE and HEOR projects from design to reporting - Draft and refine study protocols, statistical analysis plans (SAPs), and final reports - Coordinate and review additional analyses such as patient‑reported outcomes and economic evaluations - Supervise external vendors and contractors, ensuring adherence to statistical standards and project deadlines - Continuously improve analytical procedures by applying advanced statistical techniques - Ensure data integrity, reproducibility, and compliance with regulatory requirements **Required Skills** - Advanced proficiency in statistical programming (SAS, R, or equivalent) - Strong analytical and problem‑solving abilities - Excellent written and verbal communication skills for drafting reports and presenting findings - Ability to work independently and manage multiple projects simultaneously - Familiarity with clinical trial design and regulatory standards in pharma/Biotech **Required Education & Certifications** - Master’s degree or higher in Biostatistics, Statistics, Mathematics, or a closely related field - Prior experience in statistical roles within pharmaceutical, biotechnology, or clinical research settings - Knowledge of RWE or HEOR study methodologies (Note: Additional certifications in statistical software or data science may be advantageous.)

England, United kingdom

Remote

09-02-2026

Company Name

R&D Partners

Job Title

Associate Scientist, Downstream Process Development

Job Description

Job title: Associate Scientist, Downstream Process Development Role Summary: Support the development, scale‑up, and pilot‑scale production of biologic programs through execution and optimization of downstream purification steps. Operate and troubleshoot purification processes, collaborate with upstream teams, and contribute to process improvement and technology adoption. Expectations: Hands‑on laboratory work, cross‑functional collaboration, data‑driven decision making, safety‑first mindset, consistent communication of results, and capacity to work in a dynamic, fast‑paced environment. Key Responsibilities: - Plan and execute downstream purification and scale‑up activities (filtration, chromatography, TFF, depth filters). - Support upstream operations to ensure seamless end‑to‑end process flow. - Collect, analyze, and interpret process data; prepare concise summaries for meetings. - Maintain laboratory readiness: equipment upkeep, analytical instrument support, consumable inventory. - Present findings and process insights in group meetings and cross‑functional discussions. - Communicate technical information clearly to colleagues across all levels. - Foster a collaborative, solutions‑focused teamwork culture. - Uphold strict safety standards in all laboratory and pilot‑plant operations. Required Skills: - Practical experience with downstream purification (centrifugation, chromatography, TFF, depth filtration). - Proficiency in AKTA system operation and UNICORN programming. - Chromatography column operations knowledge, including resin packing/unpacking for 4.4–30 cm ID columns. - Strong verbal and written communication, technical writing, and documentation skills. - Ability to work effectively in cross‑functional teams and adapt to dynamic workflow. - Self‑motivated, organized, and capable of scientific problem‑solving. Required Education & Certifications: - Associate’s degree + 2+ years industry experience in purification techniques, **or** - Bachelor’s/Engineering degree in Chemical/Biochemical Engineering, Biochemistry, Biology, or related field + 1+ year relevant experience. Preferred (not required): - Experience with pilot‑plant operations for biologics in a single‑use facility. - Familiarity with cGMP, technology transfer, plant operations, and bioprocess scale‑up principles.

Foster city, United states

On site

Junior

18-02-2026