Study Director
About this role
Summary
MedPharm is the world’s leading contract provider of topical and transdermal product design and formulation development services. MedPharm are experts at reducing risk and accelerating development times for generic and proprietary pharmaceutical customers through their unique, cost-effective and industry-leading performance testing models. Well established as the global leaders in dermatology, nail, mucosal membrane, and transdermal product development, MedPharm can also offer innovative solutions for ophthalmic and airway preparations recognised for their scientific rigour by regulators and investors. MedPharm has fully established Centres of Excellence in the USA and the UK.
The Role
We are looking for a Study Manager to oversee and lead studies associated with formulation development and development of project proposals. This role would suit a current Study Director or somebody within a similar role. You will be reporting to the Head of Formulation Study Management and work closely with our Project Management and laboratory teams.
What does a Study Manager do?
- Prepare and amend study plans, testing protocols, reports, study updates and study related documents
- Communicate the progress of studies to the Project Manager and other internal stake holders including any amendments or deviations that have been made
- Review study data in collaboration with our scientists
- Review literature in preparation for studies and regularly update knowledge in relevant areas
What we know we need
In addition to having strong attention to detail, you must be responsible and demonstrate excellent communication and teamwork skills. The successful candidate will strive to attain in-depth knowledge of MedPharm procedures and understand the importance of study activity. If you thrive in fast-paced working environments that require a professional with drive and exceptional analytical skills, then you could be our ideal candidate.
MedPharm will send all communication using our company email address, which includes our official signature, and requires you to complete an online application as part of the process.
MedPharm is unable to offer any form of visa sponsorship at this time.
Company at a glance
MedPharm is a specialized CDMO focused on the development, testing, and manufacture of topical and transepithelial drug products.
We partner with pharmaceutical and biotechnology companies to advance innovative therapies from early development through clinical and commercial manufacturing. Our integrated capabilities span formulation development, analytical and bioanalytical testing, research biology, IVRT and IVPT studies, clinical trial material manufacturing, scale-up, and commercial manufacturing.
With expertise across multiple routes of delivery, including skin, nail, eye, respiratory (nasal and lung), and mucosal applications, MedPharm helps sponsors overcome complex development challenges and generate the data needed to make confident decisions throughout the product lifecycle.
Backed by more than 25 years of experience, specialized research models, and deep regulatory expertise, we combine scientific insight with practical execution to help accelerate development and support successful commercialization.
From concept to commercialization, MedPharm helps transform promising drug products into patient-ready therapies.
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