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

Senior Clinical Affairs Specialist

Munich
Germany
65,000EUR - 80,000EUR depeding on experience
Senior Clinical Affairs Specialist Are you interested in joining an award-winning company who are innovating in the field of cardiotherapy? Are you experienced with pre-market and post-market clinical studies for active medical devices up to class III? We're currently supporting a client in the medical device industry who are head-quartered just outside of Munich and are looking to strengthen their Clinical Affairs function. This is a hybrid position, so you must be accessible to the site. Could you be their new Senior Clinical Affairs Specialist? Tasks Responsible for the strategy and execution of clinical evaluation for medical devices up to Class III Look after the conception and the evaluation of follow-up studies Collaborate with clinical partners for various research projects Provide scientific input while supporting other areas of the organization Provide mentorship and sharing your expertise with colleagues Your profile Degree in a technical or scientific field, ideally in the direction of medical technology Several years of experience in clinical evaluation and follow-up of active medical devices up to class III Solid foundational knowledge of relevant regulatory and normative requirements (MDR, ISO 14155, MDCG Guidance etc.) Team player who can also work independently Eager to learn attitude and willingness to share your knowledge Fluency in German and English 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  

Read our Blogs

11. 01. 2021

Optimizing your CV in the Medical Device Industry

David James, our CEO recently caught up with our Medical Device Recruitment Team at Adaptive Life Science, Rebecca Stevens and Hollie Barry, where we discussed all things in relation to CVs in the MedTech industry!The structure is an easy fix. It is the content which truly differentiates you and gives you a competitive advantage to stand out to employers. Our goal is to demystify the Life Science CV to give it the substance that will make an employer stop and want to speak with you.From the common, and often easily avoidable, mistakes that we see in CVs throughout the industry, how to make your CV stand out, and reflect your suitability for a dream role!What common mistakes do you see on CVs in the Life Science industry?Rebecca: The most pertinent aspect of your CV is clarity and often there is not enough information on positions and industry experience. No two Medical Device companies are the same, not by structure, role or responsibility, so don’t assume that an employer will have a holistic understanding of what you do without proper explanation. We have spoken to Specialists who are leading teams of 5+, and Senior Managers with 10+ years who don’t have any management responsibility. The job title is not enough to go by, so make sure you are including your responsibilities and why you were hired for the role – what have you contributed to the department?The most common pitfall we see with medical device CVs is the missing buzzwords that employers will be looking for, to ensure that you know your standards and relevant regulations. Don’t just write about registrations – elaborate on the geographical markets, classes, therapeutic area, active or non-active products, software, IVDs etc... It is great if you are the business process owner for risk management, but make sure you include that you are working in accordance to ISO 14971. These small steps will quickly grab employer attention and lead to arranging an interview.Hollie: Sometimes CVs are just not specific enough – if 90% of your works focus is UDI/labelling, then write this. Don’t mislead an employer and be honest about your limitations, but instead emphasize the areas where you can deliver immediate value to them. If you’re applying for a role, always read the job description and if there are any applicable skills that you bring that aren’t already listed on your CV… add them! Some fool proof things to include but are not limited to: training accreditations (stay up to date), degree and particular relevant focus topics/thesis work, specialist focuses (CAPA/PMS/QMS Documentation etc..) International Standards, markets, MDD/MDR involvement and classes of devices.How do you make yourself stand out as a junior candidate with limited experience?Rebecca: Don’t devalue your experience and trainings received. Include everything, even if only a small part of your role, e.g. sometimes candidates only talk about their experience with non-active devices but on further investigation have worked on one active device and therefore have some knowledge on the electrical standard EN 60601 – it opens up the job market so much further.Hollie: In this case, it’s always a good idea to add any relevant internships you’ve undertaken – include the skills gained from these and any interesting responsibilities you had.How can you make your CV stand out to a recruiter on LinkedIn?Rebecca: Again, always ensuring that you have the relevant buzzwords or skills listed on your profile and make use of the specific skills section. Ensure that the industry is correct (Medical Devices or Biotechnology or Pharma etc...).Hollie: Think of your LinkedIn profile as an online CV, adding a clear and concise description of your responsibilities and focus points is so beneficial and just making sure that you update your skills regularly to reflect your experience. The more detail you share, the more chance you have of receiving actually relevant job enquiries. As an example, I recently spoke to a candidate with the title ‘Quality Manager’ for an ophthalmic medical device company and I had to decipher what his responsibilities were based off the title as there was no further information for me to use. Turns out – he was pretty hands on in registrations and quality was only 20% of his daily focus! If you can share more, it helps us get it right first time.How do you make your CV stand out for a management position?Rebecca: This is easy if you have already been managing and have direct reports or had reports in the past, although we do speak with professionals who are managing teams with full CVs not mentioning their team or number of direct reports. If not and you’re aiming for your first leading position, add any mentoring experience, project leading, supporting interns. Some companies will be open to this and provide the opportunity to develop these skills, but you need to make it easy for them to say yes by highlighting anything relevant.Hollie: I agree, I often speak with candidates who mention that they’ve been training/mentoring others in the team or providing their specialist skills to help the team in a certain area or even managing projects, yet it’s just not listed on their CV. It’s always worth adding any experience you’ve had in these areas especially if you’re aiming for that management/team lead role!What should I include on my CV?Rebecca: Training and accreditations, your degree and any relevant focus topics/thesis work/International Standards, geographic markets, MDR/IVDR involvement, Quality – are you specialising in one phase of the life cycle? Did you set up QMS from scratch or just maintenance? Employers will only have a few moments to review the CV, so this needs to be clear.Hollie: All of the above, and also confirming what classes of device that you work with? What kinds of device - active or non-active, implantable? Make it clear. Are there any projects you’ve worked on that you’re particularly proud of? Focus on the hard skills and less on the soft skills as these will be observed in the interview.It’s a good idea to always keep your CV up to date, whether you are actively looking for a new opportunity or just keeping an eye on the market.We hope that our advice has been helpful to you in some way but we’re also here to assist if you would appreciate some more specific feedback on your newly updated CV. There is no cost to our service, and we will share our honest advice to help put you in the best position for securing that interview! Rebecca Stevens - Global Life Science Recruitment Managerrebecca.stevens@adaptivelifescience.comHollie Barry - Life Science Head-hunter and Candidate Consultanthollie.barry@adaptivelifescience.com 
18. 07. 2019

Why work in the Medical Device Industry?

The global medical devices (MD) market will see a steady growth over the coming years with the sales revenue and international trade value expected to exceed $550 billion and $300 billion respectively by 2020 driven by aging population, increasing healthcare expenditure and technology advancement.But what is it like to work in such an industry, one heavy in regulation but still able to move at a lightening pace. Where companies are bought on the strength of an idea, but only have a small window before competitors strike. A truly global industry searching for the tools to allow us to prolong life…A medical device is any device intended to be used for medical purposes. What differentiates a medical device from an everyday device is its intended use. Medical devices benefit us by helping health care providers diagnose and treat us or by helping us overcome sickness or disease, improving our quality of life. Significant potential for hazards are inherent when using a device for medical purposes and thus medical devices must be proved safe and effective with reasonable assurance before regulating governments allow marketing of the device in their country.Interesting, Challenging WorkMany will tell you the work is interesting and fast paced. This in essence is what most peopelk search for, a career where they will be challenged to think of what has not been thought before and where your very ideas can shape the way we look to prolong life or treat illness.Depending on its Intended Purpose, a medical device may be classified as Class I (including Is & Im), Class IIa, IIb and III, with Class III covering the highest risk products. The higher the classification the greater the level of assessment required.From a simple syringe to the most complex artificial heart, a career in the medical device industry can give you exposure to devices we simply cannot do without up to the latest nanotechnology being utilized to save livesAmazing Company CultureMany medical devices will begin life as the idea of 1 or 2 people. Maybe it is an adaptation of an original device, a new software idea that can improve performance of existing treatment methods or a radical new idea never been seen before. Because of this there is a wide range of types of company you can work for:The up and coming Start-Up:Fast paced, crazy times…. Lets just get it done mentality needed. Often a melting pot of brilliant minds with brilliant ideas this can be an environment where you are pushed to go above and beyond but the rewards are massive.The medium sized well invested business:The idea was a winner and initial trials have gone well leading to investment. Medical Device companies can attract huge figures of investment from experienced entrepreneurs to the largest private equity firms. At these sized companies you may still only have the 1 device to be involved with but the security is greater now you have a well-funded device that is bringing in sales revenue.The global beast:These environments can be just as exciting as the start up. There could be 100’s of devices being manufactured and sold or just that 1 that every person in the world needs access to. Either way the pressure to ensure regulatory compliance and maintain the share price means work will always be fast paced and exciting, just this time on a global scale!Areas to exploreBiostatisticsClinical Data ManagementClinical DevelopmentClinical OperationsCommerical SalesDiscovery / R&DEngineeringMedical AffairsMedical InformationProductionPVG & Drug SafetyQuality AssuranceQuality ControlRegulatory AffairsTechnical OperationsComputer System ValidationFor more information on any of the areas above please contact our team at Adaptive Life Science