Our scientists will work with clinical experts to take laboratory discoveries and create treatments that are a perfect match for every patient.

The CRA I position is open to those with 6+ months field monitoring experience who want to grow their careers with Worldwide Clinical Trials.

We have an exciting opportunity for a Senior clinical research Monitoring Specialist position with one of the top medical device companies in the country.

About You: You will be a forward-thinking, people-focused individual with a passion for helping people and making a difference in the research industry.

Qualified candidates will have experience overseeing a study hands on (not just giving CRO oversight while the CRO is doing the hands on piece).

This is a very exciting time to join Cmed, as we start to leverage our already considerable expertise in the delivery of clinical trials with encapsia™.

Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Every day, we match science professionals with dream jobs that fit their skills and interests—it's the way we think job searching should be.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

- To work with our partners to ensure highly trained, well equipped and empowered Clinical Research Assistants (CRA) for all of Merck’s clinical trials

We invite you to contact us to discuss your clinical research needs or to submit an RFP for your study.

This is an excellent opportunity for those interested in being a part of multiple exciting studies in a broad range of therapeutic areas!

These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial.

You want to push the boundaries and change not just what it means to be a clinical research associate, you want to change the future.

Our mission is to bring clinical trial visits to subjects wherever they may be in order to increase convenience and compliance with study protocols.

There is also a possibility that the consultant may manage the subject eligibility committee depending on trial needs.

Candidates will need have previous clinical research experience or clinical related education.

Medical Network’s Clinical Solutions business is rapidly growing and is building the team that will create, deploy, and scale entirely new business models.

The Clinical research associate is primarily responsible for carrying out the responsibilities involved in the execution of clinical trials.