Viedoc designs engaging software for the life science industry.
By accelerating clinical trials on all levels, Viedoc's solutions support major pharmaceutical, biotech, and medical device companies, as well as renowned research institutions worldwide.
Headquartered in Uppsala, Sweden, Viedoc also has offices in America, France, Japan, Vietnam, and China.
Since Viedoc's inception in 2003, over 1 million patients in more than 75 countries have participated in studies powered by Viedoc. Who we are and what we do: At Viedoc, we design engaging software that modernizes clinical research so that necessary treatments can reach the people who need them faster.
We accomplish this by combining technology and a creative design to streamline, automate and simplify conventional processes within clinical research.
Simply put, Viedoc makes every aspect of a clinical study a bit smoother, resulting in greater discoveries that make a difference, and has the potential to improve lives.
Real change means challenging the status quo – our driving force since we started almost two decades ago.
In everything we do, we work for a healthier world, searching for better, more efficient solutions that answer to the needs of both our users and humanity.
What you will do and why: At Viedoc we are currently experiencing strong growth in Australia.
Our platform, which goes beyond basic electronic data capture (EDC) to bring electronic patient reported outcomes (ePRO), telemedicine, randomization, trial supply management, electronic trial master file, and more into a single unified platform, is gaining more and more interest among clinical trial sponsors and CROs.
With strong growth projected, we want to ensure that our customers get maximum value from the products that we offer.
The Product Specialist is responsible for supporting our customers by serving as a project manager overseeing eClinical suite builds and serving as a system subject matter expert to provide client support and technical demonstrations of the suite.
As a Viedoc Product Specialist, you will: Use your human clinical trials expertise to assist our clients (sponsors and CROs) in the management of multiple eClinical suite build projects, coordinating activities between customers, internal departments, sub-contractors (database design team), and additional partners to ensure smooth delivery of eClinical suite build Learn our product inside-out, becoming an expert in all its features including end-user features and technical design and JavaScript programming Conduct expert technical demos for potential customers Provide customer training in the use of the product suite Collect and log customer feedback to assist in driving future feature development of the product suite As a person, we would like you to be/have: A doer with a strategic, service-oriented mindset that won't rest until your assigned clients are delighted A self-motivated individual who takes personal ownership of projects with a proven track record of finding solutions to problems independently A professional team-player with strong people skills and the ability to work in a team as well as independently Ability to work remotely within Australia As a professional, we would like you to have: A bachelor's degree or higher in the life sciences, clinical research, or equivalent Two or more years of work experience within human clinical trials (e.g., clinical data manager, data programmer, or clinical database designer) at a sponsor organization or CRO OR: Relevant experience with EDC, ePRO, eCOA, or other eClinical software Excellent written and verbal communication skills in English Experience with JavaScript and/or SAS a plus Industry eClinical, Software, Pharmaceutical, Biotech, Medical Device, Consumer Health Interested?
If you want to join our awesome team, apply for the job!
Do you want to know more?
Feel free to reach out to the team member responsible for this role below.
