Project Manager - Professional Services

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:

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. That is why we are currently looking for a Project Manager to join the team.

The Project Manager is responsible for supporting our customers by serving as a project manager overseeing the new studydesigns and connected database configurations. This is a versatile role wherein you will both serve as a bridge between our developers and our clients but also as a technical advisor as well as an implementation expert.

As a Viedoc Project Manager you will:

• Use your human clinical trials expertise to assist our clients (sponsors and CROs) in the management of multiple study design projects coordinating activities between customers internal departments subcontractors (database design team) and additional partners to ensure smooth delivery of the database configuration
• Learn our product insideout becoming an expert in all its features including enduser 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 professional we would like you to have:

• A bachelors degree or higher in the life sciences clinical research or equivalent
• At least twoyears 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

As a person we would like you to be:

• A selfmotivated individual who is eager to learn the technical insandouts of our product
• A doer with a strategic serviceoriented mindset that wont rest until your assigned clients are delighted
• A professional teamplayer with strong people skills and the ability to work in a team as well as individual taking personal ownership of projects with a proven track record of finding solutions to problems independently

Industry
Saas eClinical Pharmaceutical Biotech Medical Device Consumer Health

Employment Type
Full Time

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 responsible recruiter on the original ad. Selection is ongoing so do not hesitate to get in touch.