Clinical

2020 was our Clinical Team’s busiest year, for obvious reasons.

Our consultants work with both start-ups and established global businesses to ensure their talent pools are full of experienced candidates ensuring no delay to the clinical development, or testing phases of their products lifecycle.

Be it working with some of the world’s largest CROs and Bio-Pharmaceutical companies helping them to staff international clinical trials across Phases I to IV, or working with the clinical teams within the Pharmaceutical sector to ensure all clinically developed drugs make it to market – our team have the network of clients to provide you with opportunities for your next permanent or freelance position.

Clinical Trials

  • Whether phase I or phase IV of a clinical trial, at early planning stage or putting together a PMS team as products enters the market.
  • Either way our experienced consultants use their networks built up over an extended period within the industry to deliver opportunities (permanent & freelancers) on some of the most scientifically advanced Clinical trials operating in the world.
  • If you want to accelerate your experiences then reach out to the team to discuss where we have clients in need.

Clinical Evaluation

  • Can you put a CER together to order?
  • Comfortable working on more than one at a time?
  • Does the research element of the position of the role excite you?
  • Does your current role allow you to do all of this from your home office?
  • How CER’s are produced and where the work is done has been changing and that change has been accelerated this year.
  • Speak to a member of our team to hear what our clients are doing in this field today!

PMS and Post Market Clinical Follow-Up

  • Maybe its the Post Market Surveillance team that you have built your career within?
  • You enjoy analysing how a product has impacted the market, and finding where changes can be made for future iterations of the product.
  • Our teams work with some of the most innovative companies within healthcare so if its the release of a new drug or a robotic arm we will have clients with products to excite you in your world of PMS

CRO

  • Frustrated at working on the same product day after day, year after year?
  • Then Clinical Research Organisations (CRO's) can offer you that variety.
  • Many young start-ups have very innovative exciting young ideas, they often need to outsource the research element of the product lifecycle to a CRO to ensure no delays are met.
  • Working for a CRO can give you access to some of the most forward thinking products on the market, it gives you a variety of product and people you might not have  ordinarily.
  • Reach out to the team for an informal discussion about the CRO world.

 

Active jobs

Medical Affairs Director/Senior Manager

Remote
Germany
70,000EUR - 90,000EUR
Medical Affairs Director/Senior Manager Are you an expert in Medical/Clinical Affairs in Class III Implantable Devices? Are you looking to take your next step into a leadership role? Do you want to work with a global technology leader in regenerative medicine? We are currently supporting our client headquartered in Germany to strengthen their clinical/medical affairs function. This is a remote role, so you can be based anywhere in Germany but must be willing to travel from time to time. Does this sound like your next career step? Tasks Management of a small team (2-5 employees) Ensure regulatory compliance for clinical trials and medical products on the market in accordance to MDR, TGA and FDA Pre-market and post-market clinical projects, including medical writing, CERs, PMS, and PMCFs Clinical trial project management (documentation, budget planning, collaboration with stakeholders on an international level as well as CROs) Reimbursement and compliance (Europe, especially Germany) Your profile Degree in a scientific field such as biomedical, biology, medicine, medical engineering or a comparable field of study Experience in clinical (e.g. CER), regulatory affairs, bio-medical publication or medical writing, especially for class III implants Strong communication skills and project management experience Team player who can also work independently Knowledgeable in MS Office Fluency in English, German is a bonus Please apply with your CV or contact May-Lynn Capocciama-Knecht for further details on this opportunity and additional vacancies in R&D, Regulatory Affairs and Quality Management. may-lynn.ck@adaptivelifescience.com +49 30 1663 7750 #LI-MC2  

Clinical Application Specialist

Remote
Germany
Flexible, depending on experience
Are you a specialist in the cardiovascular field? Would you like to join a dynamic healthcare company who are innovating in the field to help transform treatment options for patients? Currently, our long-standing client are searching for a Clinical Application Specialist to join them and support their mission! *Can be based in Germany, or France with 50-60% travel expected. Focuses: Act as the designated expert on the device and educate hospital workers by imparting your knowledge. Train medical professionals in the handling, insertion, and troubleshooting of the device. Oversee in-service education initiatives and one-on-one training sessions in a hospital setting. Find prospects for the adoption of therapies in conjunction with other internal teams in Clinical Affairs and R&D. Work together with R&D to offer input on new device development and feature enhancements. Arrange and participate in patient screening meetings and offer assistance with device suitability and patient selection. Requirements: 5+ years of experience in Clinical Support/Clinical Application/Field Clinical activities within the cardiovascular field OR clinical experience as a Cardiovascular Technician, Physician Assistant or CV Sonographer. Strong customer-facing experience and great communication skills. Experience in clinical engineering from roles connected to the industry that aid in clinical case assistance and development. Experience in presenting clinical and medical information. Willingness to travel (50-60%). Fluency in English is required. If you're interested in this position, please apply here and/or contact Hollie Dear at Adaptive Life Science for more information. #LI-HB1  #LI-Remot

Read our Blogs

23. 07. 2024

Key Competencies for Excelling as a Clinical Application Specialist

Key Competencies for Excelling as a Clinical Application Specialist Here at Adaptive Life Science, we assist a range of medical manufacturers in the hiring process of Clinical Application Specialists including industries such as medical devices, Biotech, and Pharma. Although, there are large differences across the industries, we have noticed that most employers are searching for candidates with similar skills. In order to assist you in separating yourself from the crowd, we have put together a list of the most desirable skills you can possess as a Clinical Application Specialist.
19. 06. 2024

Medical Device Conferences 2024 Europe (June - December 2024)

If you have not yet managed to catch a Medical Device Conference in 2024, or you are considering attending more, then this is the list for you! Here at Adaptive Life Sciences, we have selected 6 fantastic Europe-based Medical Device conferences you should attend, including online conferences for those of you who cannot find the time to travel. In order to improve readability, this list is arranged in date order.
25. 05. 2024

Relocate For Medical Device Jobs – why it can come with benefits and growth when it’s done right

Relocation and its benefits are a huge topic within recruitment, especially when speaking about niche industries like: MedTech, Aviation and Aerospace, or Mining.