EPM Scientific

EPM Scientific

Professional Services

Founded in 2012, EPM Scientific is proud to be a leading specialist talent partner for the life sciences industry.

About us

3D printing. Gene editing. Artificial intelligence. Big data. New technologies are radically transforming the way that we treat patients and cure diseases on earth and in space; fusing the physical, digital and biological worlds. There has never been a more exciting time to work in life sciences. EPM Scientific are proud to be a leading specialist talent partner in life sciences. Founded in 2012, we help clients solve the number one challenge: talent. Today, we provide permanent, contract and multi-hire talent solutions to support the whole product life-cycle from research and development through to market launch and pharmacovigilance. If you would like to talk to us about your current talent needs, please request a call back here and one of our specialist consultants will call you back to discuss your hiring needs: https://www.epmscientific.com/request-a-call-back

Website
http://www.epmscientific.com
Industry
Professional Services
Company size
1,001-5,000 employees
Headquarters
London
Type
Privately Held
Founded
2012
Specialties
Clinical Operations, Biometrics, Biostatistics & Bioinformatics, Clinical Development, Clinical Research & Operations, Commercial & Strategy, Discovery, Medical Affairs, Pharmacology, Quality Management, Regulatory Affairs, Science Information Technology, and Recruitment

Locations

Employees at EPM Scientific

Updates

  • New Role: Business Development Director Apply: https://hubs.la/Q0308hTf0 Location: Japan Join a leading biopharma contract development and manufacturing organization (CDMO) at the forefront of innovation in the APAC region. Our client provides cutting-edge solutions and services to the biopharmaceutical industry, ensuring the highest standards of quality and efficiency, and they are seeking a dynamic and experienced Sales Director to spearhead their expansion efforts in Japan and Korea. Requirements: • Proven track record of success in sales within the biopharma CDMO industry. • Strong understanding of the biopharmaceutical market in Japan and Korea. • Ability to work independently and as part of a global team. 💡Learn more about this #opportunity by applying.

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  • New Role: Site Head Apply: https://hubs.la/Q02_pH3H0 Location: Taiwan Our client is a top-tier global pharmaceutical company, driving medical innovations that shape healthcare outcomes globally. They are seeking a visionary Site Head to lead and inspire the site operations in Taiwan. This role is crucial in ensuring the highest standards of efficiency and quality, significantly contributing to the production of critical treatments for patients worldwide. Requirements: • 10+ years of experience in the pharmaceutical industry. • Proven experience with regulatory inspections, including US FDA and EMA. • Strong leadership experience, managing over 200 full-time employees across production, manufacturing, and engineering teams. • Fluent in English and Mandarin preferred. 💡 Learn more about this #opportunity by applying.

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  • New Role: Director of Clinical Operations Apply: https://hubs.la/Q02_qc8M0 Location: Boston, MA Salary: US$180000 - US$220000 per year We are working with a company looking for a Director of Clinical Operations to lead and oversee all clinical trial activities for oncology programs. This role is critical in ensuring the successful execution of clinical trials, from early-phase studies through to late-stage development. The Director will work closely with cross-functional teams, including clinical research, regulatory affairs, and data management, to drive the development of innovative cancer therapies. Requirements: • Advanced degree in life sciences, nursing, or a related field (PhD, MD, or equivalent preferred). • Minimum of 10 years' experience in clinical trial management, with at least 5 years in a leadership role. • 10 years minimum in the oncology therapeutic area and clinical development processes. 💡 Learn more about this #opportunity by applying.

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  • New Role: Senior Director, Clinical Quality Assurance Apply: https://hubs.la/Q02-HsyG0 Location: Princeton, PA Salary: US$260000 - US$280000 per year We are working with a biopharmaceutical firm dedicated to creating innovative bi-specific and multi-specific antibodies, along with antibody-drug conjugates (ADCs), aimed at cancer treatment. The company's ultimate mission is to develop biologics that systematically target tumor microenvironments, directly combat tumors, and stimulate the immune system to fight against cancer. Responsibilities and requirements of the role: • 10+ years of GCP QA experience • CAPA management • Provide GCP strategic leadership and Subject Matter Expertise (SME) to clinical study team • Provide GCP strategic leadership and Subject Matter Expertise (SME) to clinical study team 💡 Learn more about this #opportunity by applying.

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  • New Role: Vice President, Clinical Operations Apply: https://hubs.la/Q02ZRxfC0 Location: Boston, MA Salary: US$300000 - US$350000 per annum We're working with a company looking for a VP of Clinical Operations to take over their clinical operations team, leading them to success in the oncology and immunology space. Since being founded in 2016 they have raised over 1 billion dollars. With this investment they have three years of cash runway. Requirements: • 7 years of senior clinical operations leadership experience in a small biotech environment • 15 years of experience on the sponsor side of biotechs • Immunology and oncology experience desired 💡 Learn more about this #opportunity by applying.

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  • New Role: Director DMPK Apply: https://hubs.la/Q02Z1V9C0 Location: California Salary: US$200,000 - US$230,000 per year This company, dedicated to discovering and developing groundbreaking therapies to revolutionize cancer treatment, is seeking a Director of DMPK. Their team, consisting of experienced leadership and a renowned scientific founder, focuses on translating innovative research into new therapeutic solutions. Key Responsibilities: • Lead DMPK efforts in support of drug discovery and early development for small molecules, working closely with the biology and chemistry teams. • Report to the Executive Director of Preclinical R&D, collaborating with multifunctional teams across DMPK, biology, and chemistry to advance projects from discovery through early clinical development. Qualifications: • Significant experience in a leadership role within a multifunctional DMPK group at a pharmaceutical company. • Proven ability to manage and oversee ADME/PK studies and provide technical leadership across multiple projects. 💡 Learn more about this #opportunity by applying.

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  • View organization page for EPM Scientific, graphic

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    We are excited to announce that EPM Scientific will be attending MEDICA - Leading International Trade Fair in Düsseldorf on Tuesday 12th November! One of the largest medical B2B trade fairs in the world, the event will share some of the latest innovative products and services in the evolving healthcare sector. Representing EPM Scientific and keen to connect with new and familiar faces are: • Beth Frost- Associate Vice President • Conor O'Sullivan- Consultant If you can’t attend but would like to discuss how EPM Scientific can support your hiring needs, please request a call back here: https://hubs.la/Q02XfWkj0

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  • New Role: VP Regulatory Affairs Apply: https://hubs.la/Q02X8hYg0 Location: San Francisco, CA Salary: US$330,000 - US$365,000 per annum A rapidly growing biotech in CA is seeking a highly experienced regulatory affairs professional to join their team. This company has seen massive growth over the past decade and just had an incredible data readout. They are excited to welcome on a new member of the leadership team to oversee the RA functions and lead the NDA process through launch. Requirements: • 15+ years of experience in regulatory affairs in biopharma/biotech/pharma • Advanced degree preferred (MD, PhD, PharmD, MS) • Previous NDA and small molecule experience is desired • Has experience managing multiple assets in a product pipeline 💡 Learn more about this #opportunity by applying.

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