Project Manager TransCelerate Shared Investigator Platform

Basel-Stadt  ‐ Vor Ort
Dieses Projekt ist archiviert und leider nicht (mehr) aktiv.
Sie finden vakante Projekte hier in unserer Projektbörse.

Beschreibung

Harvey Nash is looking for a Senior Project Manager: TransCelerate Shared Investigator Platform & Investigator Registry for a 18 + month project in Switzerland.

The role is for an experienced professional to successfully manage a global IT project within Pharma Clinical Operations.

You are responsible for

. Developing project charters, comprehensive plans, budgets, success criteria, metrics, status reporting, communications and other deliverables to ensure all success factors have been considered
. Proactively managing project towards achievement of business objectives while adhering to agreed scope, time, quality and budget; may managing resources directly to execute project activities
. Anticipating critical activities and risks, identifying issues and demonstrating initiative to appropriately escalate and resolve
. Formulating risk mitigation strategies and recommend solutions
. Effectively communicating progress, status, dependencies and risk to stakeholders so that necessary corrective actions can be taken to keep project on track
. Demonstrating leadership and communicating in a way that is motivating, optimistic and pragmatic; fosters teamwork, collaboration and action
. Working with a Business Project Manager based in San Francisco
. Working with a vendor for all vendor-owned implementation activities who are working remotely offsite (based in EST or Asia)
. Partnering with others to develop and implement best practices for project management, development life cycle; maintaining templates, guidelines and process documentation
. Being a resource for understanding the necessary steps (eg investment rational, project management, change management, post project evaluation) to go from inception to realization of better business outcomes
. Building strong partnerships and relationships, across the organization and externally, that lead to the highest levels of collaboration and effectiveness
. Ensuring compliance to clients Project Management Methodologies and Computer Systems Validation (CSV) SOPs

Requirements

. Proven experience with 8 plus years managing a diversity of IT projects preferably in clinical investigator site portals and integration projects
. Ability to manage the project across global locations/time zones and to travel internationally as needed
. Excellent oral and written English communication skills, as well as presentation and facilitation abilities
. Very strong working knowledge of formal project management, tools and techniques
. Proven experience with a variety of techniques for requirements elicitation, analysis and definition (eg functional specifications, business process engineering, data flow diagrams, use case analysis)
. Ability to see the interrelationship of a project across "the big picture" and understand its dependency on other projects in the program as required
. Demonstrated success communicating across a variety of audiences, including business people and technologists (both up and down the organization)
. Experienced managing off shore contract resources
. Experience within the Pharma industry, specifically implementation and adoption and/or integration of applications such as investigator site portals solutions that support Clinical Operations would be highly preferred but is not a must have
. Experience deploying CSV and GxP validated systems to a globally distributed stakeholders and end-users preferred

Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred) to (see below) For further details feel free to call me. I am looking forward to receiving your application.

Start
28/04/2016
Dauer
18 months
Von
Harvey Nash IT Recruitment Switzerland
Eingestellt
11.04.2016
Projekt-ID:
1107945
Vertragsart
Freiberuflich
Um sich auf dieses Projekt zu bewerben müssen Sie sich einloggen.
Registrieren