MMS Holdings is an award-winning clinical research organization (CRO) with over 18 years of experience, specializing in complex trial data analysis and regulatory submissions. Leveraging AI technology and a data-driven approach, MMS offers comprehensive services including clinical strategy, regulatory affairs, biostatistics, and pharmacovigilance. With a global presence and industry-leading customer satisfaction, MMS is a trusted partner for pharmaceutical and biotech companies.
Open Positions
Senior Quality and Compliance Specialist (Remote)
College graduate, 5-7 years of experience, expertise in CROs, scientific data, and drug development process
Study Design Statistician - SA (Remote)
Bachelor's degree in mathematics or statistics, 5-7 years of experience in medical statistics, experience in SAS and/or R statistical software packages
Senior Medical Writer (Remote)
At least 3 years of pharmaceutical experience, 3-5 years of regulatory writing experience, and substantial clinical study protocol experience
Senior Medical Writer (Remote)
3+ years of industry experience, Bachelor's degree, and exceptional writing skills
Senior Nonclinical Writer (Remote - UK)
BS in pharmacology, toxicology, biology or chemistry, or related field, with 2+ years of pharmaceutical regulatory nonclinical writing experience and strong writing and analytical skills
Principal Medical Writer (Remote - UK)
6+ years of regulatory writing experience, substantial clinical study protocol experience, and excellent organizational skills required
Study Design Statistician (Remote)
Bachelor's degree in math/stats, 5-7 years of experience in medical statistics, experience in SAS/R, and good communication skills
Senior Quality and Compliance Specialist (Remote)
College graduate, 5-7 years' experience in GCP regulated industry, expertise in CROs and scientific data
Senior Medical Writer (Remote - UK)
3+ years experience in pharmaceutical industry, 3-5 years regulatory writing, substantial clinical study protocol experience
Nonclinical Writer
BS + in pharmacology, toxicology, biology or chemistry, or related field, with industry experience within regulatory writing, regulatory affairs, laboratory sciences, quality assurance/control
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