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

Project Manager III - Hybrid

Contract

Project Manager III- Hybrid only. Tucson, AZ No Remote work. Job Summary: Responsible for all aspects of various projects of a moderately complex nature. Interfaces with all areas affected or supporting the project. Responsible for assembling project time, assigning individual responsibilities, identifying appropriate resources needed, and developing schedule to ensure timely completion of project. Monitors projects from initiation through delivery including monitoring budget/spending. Responsibilities: Manages project team information to support project team, LCT and/or LCC decision making. Accountable for quality implementation on projects in the following areas: Project risk management; Critical path analysis; Scenario creation and analysis; Budget; Robust planning.…

Read More..

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…

Read More..

Senior AD Epidemiology - Remote

Contract

Job Title: Senior AD Epidemiology Duties: Collaborate to design, execute, and oversee high-quality epidemiology/RWE studies, and ensure that results are effectively communicated to key internal and external audiences Review and give technical input on RWE/epidemiology studies, as well as external publications, critical review assessments, and other documents Collaborate to develop timely, high-quality epidemiology/RWE sections of regulatory documents for agencies worldwide Provide epidemiology/RWE methods advice to colleagues from other functions/regions within BI Communicate effectively about global RWE strategy and study results with various internal stakeholders Skills: Trained Epidemiologist, with experience designing, implementing, and overseeing epidemiology/RWE studies using one or more different…

Read More..

Senior Researcher

Contract

Description: Principal Researcher Contract to Perm Position is a non-Ph.D. position Applicants will be provided the opportunity to actively participate in client's discovery and development of Client oncology therapeutic bispecific antibodies, antibody drug conjugates, and other biologic-based molecules. This research position will utilize tissue culture and molecular biology techniques to generate Client antibodies, bispecific antibodies, antibody drug conjugates, and therapeutic biologics to contribute to client's oncology biologics pipeline. The role of a Principal Researcher in the Biologics Discovery & Development department is a dynamic role requiring a willingness and ability to learn new laboratory techniques, instrumentation, and software. Applicants must…

Read More..

Specialist, Quality Assurance Release

Contract

Job Title: Specialist, Quality Assurance Release Duties: Review and approval of batch records of in process and finished biological product. This position would review documentation for Good Documentation Practices and against established SOPs/standards. Resolves minor / major issues found during documentation review and identifies deviations as applicable. Required Skills: GMP

Read More..