eCOA Project Consultant Medidata
Iselin, NJ

Job Description

Medidata is leading the digital transformation of life sciences with the world's most-used platform for clinical development, commercial and real-world data. Powered by artificial intelligence and delivered by #1 ranked industry experts, the Intelligent Platform for Life Sciences helps pharmaceutical, biotech, medical device companies and academic researchers accelerate value, minimize risk and optimize outcomes. Medidata serves more than 1,000 customers and partners worldwide and empowers more than 100,000 certified users every day to create hope for millions of patients. Discover the future of life sciences: www.medidata.com

We know that diverse teams win and are fully committed to selecting leaders and employees that represent the markets in which we operate. We are still led by our Co-founders, Tarek Sherif and Glen de Vries, and have global operations in US, Europe and Asia with over 2000 employees.

Your Mission:

The Project Management Function is responsible for the overall relationship management of client accounts and day to day activities.

The Project Management Function is responsible to ensure that Medidata is able to deliver quality ECOA projects and services on time and within budget through effective management of Medidata resources.

* Management of one or more projects with a focus on delivery of the scope on time, within budget and with a high quality outcome
* Provide financial management activities for one or more project budgets as well as execution of Statements of Works and Change Orders
* Generate ASOW requests and PSCAs in order to manage scope changes
* Provide input to Professional Services Proposals
* Maintain appropriate project/client documentation within e-binders for one or more projects/clients
* Maintain high client satisfaction by providing proactive communication and issue management
* Provide guidance and consulting to clients around the best use of the Medidata Applications
* Is Subject Matter Expert (SME) in at least 2 Medidata Applications through the delivery of workshops and other consultancy activities
* Manage assigned project resources
* Assure compliance with Medidata's standard project management methodologies and Medidata SOPs
* Provide mentorship and guidance to all assigned project members

Your Competencies:

* Good understanding of clinical research (pharma, device and/or biotech sectors) and a solid understanding of Clinical Research SaaS technology
* Excellent verbal/written communication and organizational skills
* Excellent computer skills, public speaking, presentation and teaching skills
* Proficient with MS Office suite, Word, Excel and PowerPoint
* Excellence with MS Project, project development and management
* Self motivated, able to work remotely and able to assume responsibility in a professional manner
* Is proficient in the use of all relevant Medidata internal systems
* Travel expectations up to 20% - 30%, national / international
* Valid driver's license required

Your Education & Experience:

* Related experience with univesity degree (analytic discipline a plus) or an advanced degree without experience or equivalent work experience.
* Relevant experience in clinical/biomedical and/ or software development environment preferred
* Electronic Clinical Data Management (eCDM) software consulting experience desirable

Medidata is making a real difference in the lives of patients everywhere by accelerating critical drug and medical device development, enabling life-saving drugs and medical devices to get to market faster. Our products sit at the convergence of the Technology and Life Sciences industries, one of most exciting areas for global innovation. Nine of the top 10 best-selling drugs in 2017 were developed on the Medidata platform.

Medidata's solutions have powered over 14,000 clinical trials giving us the largest collection of clinical trial data in the world. With this asset, we pioneer innovative, advanced applications and intelligent data analytics, bringing an unmatched level of quality and efficiency to clinical trials enabling treatments to reach waiting patients sooner.

EEO Statement

EMEA:

MDSOL Europe Ltd is an equal opportunity employer. We welcome all applications irrespective of race, gender, gender reassignment, age, religion or belief, relationship status, pregnancy/maternity, sexual orientation or disability.