Do you have a Burning Desire to Prove your Mettle?

We’re a front runner in acquiring talent and developing strategies for a futuristic digital business model.

Every step we take forward is a testimony of our perseverance for your holistic development and for excelling in your career in cultural diversity.

Here at Maxis Clinical Sciences, you not only build your career but seek your ambitions. We endeavor to nurture your indigenous talent in a world-class environment where you’ll always thrive, and seek an enriching & rewarding career. Here we empower you to innovate with your business ideas and follow them through. Every training we provide reflects our vision and imprint of our organizational roadmap to seek development opportunities in every profile at Maxis Clinical Sciences.

Passion, perseverance, and poise are the best superlatives that describe us!


Current Openings

Quality Associate II

Direct Placement

Job Title: Quality Associate II Direct Hire with the client. Primary Duties & Responsibilities: Understand quality procedures, safety procedures and cGXP procedures and systems. Review in-process batch records/manufacturing run sheets to support product release. Conduct training for cross-functional departments. Lead timely investigations for donor lookbacks. Conduct SOP and form revisions, including bi-annual reviews. Review and approve records in the quality system (i.e. CPAs, CSRs, LIRs, ORs, SCARs). Identify and assess regulatory and quality risks in operations according to applicable regulations and company quality practices. Lead/write investigations, determine root cause(s) and effective corrective actions, communicate, and report product quality problems in…

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SAS Programmer - Must be Onsite

Full Time/Contract

Position: Senior SAS Programmer Full Time Role - Would need someone who can be onsite. Provide statistical programming support for clinical trial data reporting under the general guidance of a biostatistician . Develop SAS programs that generate tables, listings and figures and derived datasets that summarize results for clinical trials. Contribute to the development and implementation of programming and reporting standards. Contribute to the development of a macro library. Work closely with data management to assure data quality and consistency. Provide occasional analytical support under the supervision of a biostatistician . These efforts must meet company objectives and satisfy regulatory GCP…

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