EPM Scientific

New Role: Director/Senior Director, DMPK and Clinical Pharmacology Apply: https://hubs.la/Q02N7R030 Location: San Francisco, USA Salary: US$230,000 - US$300,000 per year This company is seeking an experienced and motivated Director to Senior Director of DMPK and Clinical Pharmacology to provide expert guidance on clinical pharmacology programs supporting drug discovery and clinical development. In this role, you will be responsible for authoring clinical protocols, study reports, and analyzing data (exposure/efficacy/safety) to support the development and registration of products. Requirements: • PhD or PharmD in Clinical Pharmacology, Pharmacokinetics, Pharmaceutics, or related field • Extensive experience in clinical pharmacology with proficiency in model-based analyses (PK/PD, ER, QSP, PBPK) • Knowledge of drug development processes and experience with regulatory submissions (IND, NDA) 💡 Learn more about this #opportunity by applying.

EPM Scientific is delighted to announce that we are hosting a panel discussion in October! Join our life sciences industry experts and special guests as they talk through the topic of ‘Clinical Trials In The Age Of AI’ on Thursday October 24th in our Berlin office. We can reveal that our first guest speaker will be Marco Schmidt, Chief Scientific Officer at https://hubs.la/Q02MKyJX0. More details of the schedule will be revealed shortly. If you are interested in attending the event, please contact Hashan A. [email protected].

New role: Global Quality Consultant 📍 Switzerland: https://hubs.la/Q02MnSv-0 Job overview: This company is seeking a highly independent and experienced Global Quality Consultant with a strong background in compliance within cell therapy and biopharmaceuticals. The role focuses on ensuring compliance across enterprise-level QMS, with a particular emphasis on supporting system updates and enabling functions. Requirements: • Extensive experience in cell therapy and biopharmaceutical compliance • Proven capability to operate independently and lead compliance functions in a global environment • Experience with launching cell therapy products • Proficient in English; additional languages are a plus

New role: Clinical Data Manager 📍 London, England: https://hubs.la/Q02JKzvy0 Job overview: A global pharmaceutical group, dedicated to developing and commercialising treatments for patients with genetic, metabolic, systemic, and acute life-threatening disorders, is looking for a Clinical Data Manager to join its team. Requirements: • Bachelor's degree or equivalent experience in mathematics, science, or a related field • Proven experience in the pharmaceutical or biotech industry within clinical research and/or clinical data management • Good knowledge of international clinical research regulations and requirements (ICH/GCP) • Experience with clinical trial databases and applications, clinical data flow, data review, and eCRF design

Have you read our FTC Non-Compete Ban guide yet? Discover the opportunities and challenges the Federal Trade Commission’s (FTC) new ruling prohibiting non-compete agreements will bring for life sciences organizations, and read advice from Jae Yoo, Executive Director, and Luke Newton, Managing Director at EPM Scientific. Download your copy today: https://hubs.la/Q02JJB9t0

New role: Senior Supply Manager 📍Switzerland: https://hubs.la/Q02JKbHv0 Job overview: This company is seeking a highly experienced Senior Supply Manager on a 12-month contract basis to lead and manage supply chain projects, with the potential for a permanent position. Requirements: • 5 to 7 years in the pharma and biotech industry • Proficient in SAP - Integrated Business Planning (IBP) • Fluent in English • Strong understanding of supply chain management, project management, and tech transfer for CMOs

New role: Quality Engineering Specialist 📍 Switzerland: https://hubs.la/Q02HZvkY0 Job overview: This company is seeking a highly skilled and dedicated Quality Engineering Specialist for a 6-month contract, to start as soon as possible. The role holds all quality related responsibilities for daily qualification activities on technical facilities, equipment and systems. Requirements: • Experience in biotechnology or pharmaceutical environment • QA Qualification • Knowledge on FAT/SAT/IQ/OQ/PQ • Proactive, with good communication skills and able to work in a multidisciplinary team towards a common goal • Fluent in English (spoken and written)

With the potential to affect 30 million Americans, do you know how the new Federal Trade Commission’s (FTC) ruling prohibiting non-compete agreements will impact your business? Don't worry, our latest guide explains the resulting challenges and benefits if the changes are allowed to come into effect. With expert insights from Jae Yoo, Executive Director, and Luke Newton, Managing Director at EPM Scientific, you can make sure you are prepared ahead of the ruling in September. Download your copy here: https://hubs.la/Q02HZ3pM0

Looking for hourly rate averages for clinical operations contract roles in Europe? Download EPM Scientific's new Clinical Operations Rates Guide: https://hubs.la/Q02GVGRq0 Featuring current hourly rate benchmarks for Clinical Research Associate, Clinical Trial Manager, and Clinical Project Manager roles for over 20 European countries, download this indispensable resource today. #LifeSciences #ClinicalOperations #HourlyRates

New role: Field Clinical Specialist (m/f/d) 📍 Germany: https://hubs.la/Q02G2l8m0 Job overview: Are you passionate about making a significant impact on patients' lives through your clinical expertise? This company is seeking a dedicated Field Clinical Specialist to join their team and drive clinical excellence within the medical device sector. Requirements: • Strong clinical foundation required; demonstrated understanding of hospital environments • Prior experience or background knowledge of perfusion is preferred • Fluent in German, good English