Project Manager - Belfast

Genpact Pharmalink
13 Nov 2017
16 Nov 2017
Contract Type
Full Time
Project Manager

Contract Full Time Permanent

Reference GPPM1017

Location Belfast

SalaryCompetitive + benefits, pension, healthcare, life assurance.

Hours 40 hours per week (Monday - Friday)

Company Profile:

Genpact Pharmalink Global Regulatory Affairs combines Pharmalink's domain expertise in consulting, project support and outsourced regulatory affairs services with Genpact's global delivery, BPO, technology and analytics offerings for the global life sciences market.

Pharmalink Consulting is a highly specialized Regulatory Affairs Consultancy with a successful history spanning over 14 years. We have grown and developed our service offering through building relationships, listening to our clients' needs and adapting our ways of working to meet the changing needs of regulatory markets around the world. It is this flexibility and adaptability that we look for in all of our Consultants, which will allow us to continue to provide the level of service our clients have come to expect from Pharmalink Consulting.

The success of Pharmalink Consulting depends on its people. Capitalizing on what is unique about individuals and drawing on their different perspectives and experiences will add value to the way we do business. By accessing, recruiting and developing talent from the widest possible talent pool we can gain an insight into different markets and generate greater creativity in anticipating employee and client needs.

Working as part of the Pharmalink Consulting team gives you a career that will be varied, diverse and never dull! You will be joining a team of the best Regulatory Affairs Professionals in the industry, some of the most experienced and progressive minds. Our consultants come from a wide spectrum within the Healthcare Industry, all bringing invaluable skills and attributes that allow us to provide the best Regulatory Affairs expertise to our clients

The Role:

We currently have an opportunity for a Project Manager based in our Belfast office. You will gain invaluable experience in Regulatory Affairs submissions and Systems Management. You will work closely with upper management and Team Leads autonomously to deliver project goals for some of the world's most prestige's clients.

The Project Manager will work on various projects with exposure to some of the world's leading pharmaceutical breakthroughs. Obviously, all of our work is protected and highly confidential. The ideal candidate should have a minimum 5 year's project management experience and preferably within a science or health related industry.

Key Responsibilities:

- Integrate into client environment to effectively lead project teams while building positive professional relationships with clients and associates.
- Define project objectives, requirements, and assumptions necessary to structure a project or activity.
- Plan, schedule, and control project activities to fulfill objectives and satisfy project requirements.
- Develop and drive integrated project plans, aligning project tactics with project strategy.
- Establish, maintain, and lead high performance project teams, serving as the project advocate within the client organization. Lead, coordinate, facilitate, and motivate all associated project resources to gain alignment on project goals and deliverables.
- Lead risk management within project teams, ensuring risks have appropriate mitigation and contingency plans.
- Manage projects within established scope, schedule, and budget while meeting and exceeding IPM project management standards.
- Develop and document high-level strategies for accomplishing specific project objectives.
- Facilitate and lead effective project meetings, manage change and conflict, and develop resource planning estimates to manage project workload and productivity.
- Support project management team members to ensure success of projects while maintaining customer service focus.
- Remote role with up to 20% travel required
- Working within tight, business-critical deadlines in a highly regulated environmentEssential Criteria:
- Bachelor's degree and/or relevant Project Management qualification.
- Knowledge and application of a disciplined project management process (Six Sigma and Project Management Professional certifications are a plus).
- Exceptional interpersonal and leadership skills to effectively communicate and build relationships with a broad spectrum of audiences at all organizational levels.
- Sound technical aptitude and proven ability to grasp general knowledge of multiple disciplines and technologies with superior computer usage skills.
- Strong competencies in planning, project management, and organization with the ability to lead multiple activities and resources while maintaining a focus on quality.
- Solid analytical and strategic capabilities and business acumen along with demonstrated work ethic, integrity, and professional conduct and appearance.
- Ability to produce and present clear, concise, and professionally written communications and presentations.
- Desirable Criteria:
- Strong knowledge of Regulatory Affairs, R&D, Drug Life Cycle and Drug Development
- 5+ years of industry experience in the pharmaceutical, biotechnology, and/or similar industries.
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- For more details on our capabilities and career development opportunities, please visit URL removed
- To Apply:
- Please forward your CV to *********************** quoting referencing 'GPPM1017' in the subject line