Medicine moves forward here. So will you.
ADAMAS Consulting helps the world's pharmaceutical and biotechnology companies uphold the highest standards of quality, compliance and patient safety. Since 2007 we have partnered with organizations across GCP, GVP, GMP, GLP and Computer Systems Compliance, and we are trusted by many of the most respected names in life sciences.
We think of our work as more than auditing. At its best it is intelligence: helping clients see the compliance risks that matter most and prevent the problems that could put patients at risk. That takes sharp, independent thinking and deep expertise, which is exactly what our people bring.
Here your knowledge is valued and shared, not kept in silos. We have built a supportive, collaborative environment where professional growth is encouraged and where you can make a real impact across the industry, working alongside some of the most respected companies in the field.
Job DescriptionPlanning, preparation, conduct, reporting and follow up of various types of GCP audits according to expected quality and timelines
Executing audits based on a comprehensive understanding of all regulatory requirements and Good Clinical Practice (GCP).
Performing GCP quality assurance projects on behalf of client companies within the pharmaceutical/biotechnology industry.
BSc in Life Science preferred
Experience in conducting and leading internal and external GCP audits for a variety of stakeholders
Experience in conducting a range of service provider audits (e.g., full-service CRO, biostatistics, data management, phase I)
Experience in conducting GCP systems audits.
Experience in coordinating and managing inspection preparation activities for GCP process inspections both at the sponsor and investigator site.
Experience in conducting GCP mock inspections to Competent Authority standard considered a significant advantage.
Expert knowledge of national and international GCP legislation and guidelines
Up to 40% travel and ability to conduct remote audits
Why ADAMAS?
When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.
We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here.
Quality: we hold ourselves to the standard patients deserve.
Integrity and trust: we do the right thing, especially when it is hard.
Drive and passion: we care about the outcome, because someone is waiting on it.
Agility and responsiveness: we move quickly, because patients cannot wait.
Belonging: everyone is welcome, and every voice counts.
Collaborative partnerships: we go further by going together.
We look forward to welcoming your application.
Skills Required
- Experience conducting and leading internal and external GCP audits for various stakeholders
- Experience conducting service provider audits, including CRO, biostatistics, data management, and Phase I audits
- Experience conducting GCP systems audits
- Experience coordinating and managing inspection preparation activities for GCP process inspections at sponsor and investigator sites
- Expert knowledge of national and international GCP legislation and guidelines
- Ability to travel up to 40% and conduct remote audits
- BSc in Life Science
- Experience conducting GCP mock inspections to Competent Authority standards
What We Do
Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology. • 1,400+ highly qualified professionals • Global full-service CRO • 25+ years of experience • Therapeutic specialization in oncology • Strong expertise in rare disease trials • Robust clinical safety system • Choice of leading drug safety databases Our key services include: • Clinical Research Services • Pharmacovigilance • Medical Information • Regulatory • Medical Writing • Site Management • Study Physician Support • Biostatistics • Patient Study Support
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