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Join us.

If you have a positive and enthusiastic approach and would like to contribute to our organisation’s success, please get in touch with us. In return, we will provide a culture and working environment that is distinctive and different. We will invest in your future by offering a variety of opportunities for training, along with personal and professional development.

If you are interested in becoming part of our global organisation, please view our existing vacancies and apply below.

Current vacancies.

  • Clinical Operations Manager II

    Our ever-expanding Clinical Development division are looking for a Clinical Operations Manager II to onboard, train, coach, mentor, manage and oversee activities of our CRAs and CTAs to ensure the successful start-up, monitoring and execution of Phase I-IV trials. You will be a key contributor to the overall clinical operations team, ensuring knowledge sharing and best practices. If you want to be part of our company vision of bringing life-changing medicines to patients around the world, please click apply for more information

    VA 297PermanentHomebased UK Apply
  • CRA II

    We are currently looking for a CRA 2 to join our ever-expanding Clinical Development team in the US. You will have prior experience in study start-up, onsite monitoring, remote monitoring and associated systems CTMS, eTMF, IVRS, Safety, etc. If you would like to be a part of our company vision of bringing life-changing medicines to patients, please click apply.

    VA 320PermanentUS - Flexible, Home Apply
  • CRA II

    We are currently looking for a CRA 2 to join our ever-expanding Clinical Development team in the UK. You will have prior experience in feasibility, study start-up, onsite monitoring, remote monitoring and associated systems CTMS, eTMF, IVRS, Safety, etc. If you would like to be a part of our company vision of bringing life-changing medicines to patients, please click apply.

    VA 321PermanentFlexible/Homebased/Office/UK Apply
  • CTA II

    An excellent opportunity has arisen for an experienced CTA II, preferably with experience of working for a CRO to come and support our Clinical Development Team. We are looking for a determined and self-driven individual who wants to be part of our company vision of bringing life-changing medicines to patients around the world. For more details on this role, please click apply.

    VA 308PermanentFlexible, East Coast, USA Apply
  • CTA II

    An excellent opportunity has arisen for an experienced CTA II, preferably with CRO experience to come support our Clinical Development Team. You will have a can do and determined attitude and be a self-driven individual who wants to be part of our company vision of bringing life-changing medicines to patients around the world. For more details on this role, please click apply.

    VA 309PermanentOffice Based, UK Apply
  • CTA II (with CTMS experience)

    An excellent opportunity has arisen for an experienced CTA II with experience in managing CTMS systems, preferably from a CRO background, to come and join our Clinical Development Team. You will have a can do and determined attitude and be a self-driven individual who wants to be part of our company vision of bringing life-changing medicines to patients around the world. For more details on this role, please click apply.

    VA 310PermanentHome and Office based UK Apply
  • Patient Access Associate (German Speaking)

    We have an opening for a Patient Access Associate within our Early Access Programs (EAP) division. This is a great opportunity to join a team who are passionate about making a difference to patients’ lives. We are looking for a person who speaks German and has previous pharmaceutical/healthcare experience in a customer facing role. The ideal candidate will have strong communications skills as they will be required to work closely with Project Managers and supporting health care professionals in accessing life changing medicines for patients around the world. It is essential that the candidate is fluent in German, both verbal and written and language related work experience would be desirable. The candidate we are looking for will be committed and passionate about bringing our company vision to life and making a difference to patients’ lives. Please click apply for more information

    VA 252PermanentUK Apply
  • Patient Access Associate (Italian Speaking)

    We have an opening for a Patient Access Associate within our Early Access Programs (EAP) division. This is a great opportunity to join a team who are passionate about making a difference to patients’ lives. The ideal candidate will have strong communications skills as they will be required to work closely with Project Managers and supporting healthcare professionals in accessing life changing medicines for patients around the world. It is essential that the candidate is fluent in Italian, both verbal and written and language related work experience would be desirable. The candidate we are looking for will be committed and passionate about bringing our company vision to life and making a difference to patients’ lives. Please click apply for more information.

    VA 325PermanentUK Apply
  • Project Coordinator EAP

    We have an opportunity for a Project Coordinator to join our exciting Early Access Programs (EAP) division. You will be pivotal in supporting the Project Lead on the delivery of a number of EAPs as well as providing excellent customer service to our clients. If you want to be part of our company vision of bringing life-changing medicines to patients around the world, please click apply for more information.

    VA 299PermanentUK/US Apply
  • Project Leader

    We are currently looking for a Project Leader to join our Clinical Development division where you will lead and support the department to ensure that accounts are serviced to a high level and, when required, personally assist in the delivery of projects to ensure they are delivered on time and within budget. You will be a mentor to fellow team members and be passionate about bringing life-changing medicines to patients around the world. If you want to be part of a growing company, we want to hear from you. Please click apply for more details.

    VA 300PermanentUSA Apply
  • PVG Safety Systems Administrator

    An exciting opportunity has arisen for a PVG Safety Systems Administrator to join our Pharmacovigilance department. You will have previous safety database administration experience as well as experience in creating and validating safety reports. If you are someone who wants to be part of our company vision of bringing life-changing medicines to patients around the world, please click apply.

    VA 323PermanentLetchworth Apply
  • Qualified Person

    Our Clinical Trial Supply division are looking for a Qualified Person who will have the responsibility for maintaining Quality Assurance and Regulatory compliance within the Clinical Trial Supply (CTS) and Early Access Programme (EAP) functions. Ensuring that all regulatory and licensing requirements for CTS and EAP are met. QP release of Packaging & Labelling batches from the Ireland facility. If you want to be part of our company vision of bringing life-changing medicines to patients around the world, please click apply for more information.

    VA 289PermanentIreland Apply
  • Quality Assurance Officer (NJ, USA)

    Our expanding QA Department are resourcing a new QA Officer in NJ, USA. The right candidate will be responsible for assisting in the provision of the company’s quality assurance function, including Quality Management System *(QMS). The role will require strict compliance with current cGMP requirements and will be an integral part in driving best practice and continuous improvement. This is a great opportunity to be part of a team dedicated to high quality delivery that ultimately allows us to bring life-changing medicines to patients around the world. If you want to be part of bringing our vision to life please click apply for more information.

    VA 222PermanentNJ 08066, USA Apply
  • Real World Data Coordinator

    We have an exciting opportunity for a Real World Data Coordinator within our Early Access Programs division. In this role you will be working towards the delivery of effective and efficient Real-World Data programs. You will be a determined and driven individual who wants to be part of our company vision of bringing life-changing medicines to patients around the world. For more details on this role, please click apply.

    VA 312PermanentUK/Europe Apply
  • Regulatory Associate x 2

    An excellent opportunity has arisen for a Regulatory Associate to join our Regulatory Affairs department. Experience of working with small biotech companies would be advantageous as would be experience of writing scientific/technical documents across the entire product lifecycle. You will be a determined and driven individual who wants to be part of our company vision of bringing life-changing medicines to patients around the world. For more details on this role, please click apply.

    VA 313PermanentUK Apply
  • Senior Contract Specialist

    A very exciting and rare opportunity has arisen for a Senior Contract Specialist to join our Clinical Development division where you will be working across all studies to support the Clinical Operations team with the implementation and maintenance of all Confidentiality Disclosure Agreements (CDA), contracts, budgets and associated documents used in the clinical trial lifecycle to enable effective and efficient execution and management of all contracts for Bionical-Emas managed studies. You will be a determined and driven individual who wants to be part of our company vision of bringing life-changing medicines to patients. For more details on this role, please click apply.

    VA 315PermanentRemote/Letchworth Apply
  • Senior CRA

    We have an opening for a Senior Clinical Research Associate to join our successful Clinical Development division. You will be implementing and monitoring clinical trials on & off-site to ensure investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH-GCP guidelines. If you want to be part of our company vision of bringing life-changing medicines to patients, please click apply for more information.

    VA 277PermanentMiami Apply
  • Senior Medical Writer

    We have an excellent opportunity for a Senior Medical Writer to support our Clinical Development & Early Access divisions. This new position will be a senior-level role within our Regulatory Affairs Team. You will be a determined and driven individual who wants to be part of our company vision of bringing life-changing medicines to patients around the world. For more details on this role, please click apply.

    VA 260PermanentHomebased Apply
  • Senior Project Associate x 2

    We are currently looking for a (Senior) Project Associate to join our PMO department. You will have prior experience of at least one year as Project Support or other relevant clinical research experience, as well as good understanding of GCP, the drug development process, clinical study phases, and clinical research terminology. If you are someone who is a real go getter and wants to be part of our company vision of bringing life-changing medicines to patients around the world, please click apply.

    VA 316 & 317PermanentRemote, UK Apply
  • Senior Project Leader

    We are currently looking for a Senior Project Leader to join our Clinical Development division where you will lead and support the department to ensure that accounts are serviced to a high level and, when required, personally assist in the delivery of projects to ensure they are delivered on time and within budget. You will be a mentor to fellow team members and be passionate about bringing life-changing medicines to patients. If you want to be part of a growing company, we want to hear from you. Please click apply for more details.

    VA 305PermanentUK/Germany/Ireland/Portugal Apply
  • Senior Regulatory Manager

    A fantastic opportunity has arisen for a Senior Regulatory Manager to join our Regulatory Affairs department. Your role will entail working to deliver strategic and operational regulatory support and expertise to the Early Access Program (EAP) & Clinical Development teams, as well as to ensure efficient and compliant set-up, maintenance and close-out of Regulatory Scopes. If you are someone who wants to be part of our company vision of bringing life-changing medicines to patients around the world, please click apply.

    VA 324PermanentHomebased Apply
  • VP of Data Services

    We are currently looking for a Vice President of Data Services. This will be a pivotal role where you will support the Executive Vice President (EVP) of Clinical Development to define and implement appropriate data collection and analytic strategies and solutions for the management of worldwide Data Services activities and deliverables. If you want to be part of a growing company who are passionate about making a difference to patients’ lives, we want to hear from you. Please click apply for more information.

    VA 290PermanentHomebased UK Apply

Life at Bionical Emas.

To understand more about life at Bionical Emas, interns and staff alike give their insight into starting out within the industry and working for a Clinical Research Organisation.

How can we support you?

Our dedicated teams of experts are on hand to help should you require any additional resource or further information about our services.

COVID-19 Guidance & Measures

A statement from the Bionical Emas Group on guidance & measures regarding COVID-19 - read here

In relation to staff and visitor safety, we have full risk assessments in place for all of our workplaces. These risk assessments are revisited and updated regularly, to reflect changing risks, knowledge and circumstances, and to reflect evolving Government guidance. We have not placed the risk assessments here on the website as they would become out of date too quickly. However, you are welcome to email info@bionical-emas.com to request access to our most up to date risk assessments applicable to your needs. Please note that all our staff are notified of all applicable risk assessments and updates, along with ‘quick guides’ automatically via our e-learning system.