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Chemicals/Petrochemicals
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development
Responsibilities
. Supports direct reports in monitoring of their projects to assure company profitability and associated project goals and objectives are being met.
. Develops, implements, and monitors profitability, objectives, metrics of assigned group of direct reports.
. Identifies and implements improvements of processes within the assigned service are through review of project specific plans and their implementation recommends improvement plans to project.
. Manages resources and resource projections to ensure project teams are consistent with client needs, expectations and contractual obligations.
. Analyzes current and future project backlog in order to provide adequate resources to meet business objectives.
. Builds and aligns a technical team to perform critical operating tasks to achieve results.
. Identifies and implements process improvements and other ways to improve efficiencies.
. Provides technical oversight of the generation of project plans such as but not limited to Safety Management plans (SMP), or SAE Reconciliation plans, in close cooperation with project team during set-up phase.
. Delivers training on department related topics as well as general company processes and systems to Pharmacovigilance staff.
. Liaises with other functional managers to ensure consistency of safety management approaches within the company.
. Maintains familiarity with current industry practices and regulatory requirements that affect services provided respective service area.
. Reviews Pharmacovigilance (Reporting) Associate, Pharmacovigilance (Reporting) Specialist and/or Pharmacovigilance Assistant, Pharmacovigilance (Senior) Project Manager and Pharmacovigilance Project Lead, Pharmacovigilance Assistants, group-related project tasks provides leadership in the delivery of related services to clients.
. Ensures that staff fulfill their responsibilities in accordance with company and/or client QMS, policies, procedures, and SOPs, as applicable.
. Creates an environment that encourages learning, self-improvement and career development for staff.
. Supports the development and implementation of training for Pharmacovigilance (Reporting) Associate, Pharmacovigilance (Reporting) Specialist and/or Pharmacovigilance Assistant, Pharmacovigilance (Senior) Project Manager and Pharmacovigilance Project Lead, Pharmacovigilance Assistants, or other personnel within the assigned service area.
. Recommends and supports implementation of performance and productivity improvements within the assigned service area to ensure optimal utilization of billable staff.
. Performs metric collection and data analysis to support company efforts for continuous improvement in policies, procedures, and business processes.
. Identifies and implements process improvements through review of SOPs, processes recommend improvement plans to senior management.
. Participates in task forces to implement process improvement initiatives.
. Builds teamwork and improves process and productivity by working within and across functional areas.
. Develops company employees to ensure high quality work performance and retention of high quality employees.
. Ensures staff development and performance feedback are provided through activities such as mentorship and career development.
. Communicates team/individual goals and expectations to ensure direct reports understand their responsibilities.
. Involved in the recruiting processes for new employees in the assigned service area.
. Assists with bringing new business opportunities to the company and maintaining existing clients relationships for repeat business.
. Interacts with clients and participates in client meetings as necessary to support and maintain new business.
. As assigned, participates in business development initiatives, including presentations and proposal development.
. Ensures that timely and accurate information is submitted on all proposal efforts.
. Participates in business development initiatives, including presentations and proposal development.
. Supports direct reports and senior management during audit preparation and conduct. Responds to audit findings as needed.
. Prepares Standard Response letters, including conducting literature search, article summary etc.
. Responsible for vendor management (e.g. LPPharmacovigilance)
. Supports Qualified Person for Pharmacovigilance as required
. Travel (approximately 15%) domestic and/or international
. Management of assigned safety and/or medical information call center handling teams to ensure project and departmental deliverables are being met.
. May serve as Local/Qualified Person for Pharmacovigilance (including deputy level)
Supervision Given
. Works under general supervision and coaching for managerial task
. Works independently most of the time.
What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
Various annual leave entitlements
A range of health insurance offerings to suit you and your family's needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
Visit our to read more about the benefits ICON offers.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request.
Interested in the role, but unsure if you meet all of the requirements We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
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Date Posted: 19/10/2024
Job ID: 96883135
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.We offer a full range of consulting, development and commercialisation services from a global network of offices in 37 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.