Are you looking to join a company where your contributions truly matter, and where you’ll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO).
We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges.
With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive.
Join us at MMS and be part of a team that is shaping the future of clinical research. Discover more about our exciting opportunities and why MMS is a great place to advance your career.
Visit www.mmsholdings.com or follow MMS on LinkedIn .
Roles and Responsibilities Lead complex projects, programs and submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsors.
Can develop SAPs and iSAPs text and shells with no supervision.
Produce and present external company presentations providing industry visibility for the organization; Continually suggesting solutions to solve issues in tune with organizational direction.
Can review or develop ADAM specifications; can work with programmers and junior statisticians to resolve comments.
High technical level, Subject Matter Expert in biostatistics; willing to guide others in a variety of biostatistical techniques.
Has the ability to apply drug development knowledge during production of complex statistical analyses.
Review or create the statistical section(s) of a Sponsor’s protocol and ensure that the appropriate statistical methods are proposed for the study design and objectives.
Provide valuable feedback to the Sponsor on the statistical aspects of the study.
Prepare and review statistical methods and results sections for the CSR independently in collaboration with in-house medical writers.
Demonstrate an understanding of project management-related tasks such as timelines, scope and resource requirement estimation/management.
Perform sample size calculations for a variety of scenarios and study designs.
Can provide statistical consulting support to sponsors re study design and sample size calculations.
Ability to create randomization and kit schedules independently, collaborate with sponsor, randomization and drug supply management teams.
Job description from Brightview Senior Living About Us Overview Does being kind and compassionate come naturally to you? Do you...
Apply For This JobClearance Required: Top Secret SCI Education Required: BA/BS US Citizenship: Required Summary The MIL Corporation is seeking a Cyber Security...
Apply For This JobJob description We are seeking a detail-oriented and proactive Administrative Clerk to join our team remotely. This role plays a...
Apply For This JobJob description from Allied Universal Job Description Job DescriptionOverview Company Overview: Allied Universal®, North America’s leading security and facility services...
Apply For This JobJob description from Domino’s Job Description Job DescriptionJob Description JOB DUTIES: Operate all equipment, Stock ingredients from delivery area storage,...
Apply For This JobJob description from Soliant Job Description Job Description Degree in Radiologic Technology, Certification in Radiologic Technology (ARRT Certification), and minimum...
Apply For This Job