FSP, Project Manager: Non-Interventional Study(NIS)

at  Thermo Fisher Scientific

North Carolina, North Carolina, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate14 Nov, 2024Not Specified15 Aug, 2024N/ATravel,Powerpoint,Interpersonal Skills,Project Teams,Office Equipment,Deliverables,Tpc,Scheduling,Microsoft Outlook,Wellbeing,Excel,Leadership Skills,Business Rules,Clinical Trials,Technology,Strategy,Directives,Cultural Awareness,Diverse GroupsNoNo
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Description:

DISCOVER IMPACTFUL WORK:

We are seeking a Project Manager/Lead in our FSP, Project Management Team.

  • This role will be hired at Project Manager
  • This role is for the North America region and is remote based.

The PL Is accountable for the overall delivery of the project (quality, time, cost) on behalf of the organization. Establishes and communicates customer expectations to the project team with minimal direction. Ensures that escalation pathways are adhered to internally and externally. Leads the cross-functional project team to meet or exceed deliverables. Manages project(s) of increasing complexity (such as but not limited to: multi-service, multi-region/country, therapeutic complexity, financial scope).
this role will deliver high quality development schedules / plans based on analytical data, benchmarks and information from the Medicine / Vaccine Development & Medical Teams. This position must become a trusted partner to and interact early and closely with the accountable Team Members and the associated functional lines to build & maintain high quality project plans in the system.

EDUCATION

  • Bachelor’s degree or equivalent and relevant formal academic / vocational qualification

EXPERIENCE

  • Previous experience that provides the knowledge, skills, and abilities to perform the job
  • 5+ years of management responsibility
  • Proven leadership skills
  • Previous Non-Interventional Study(NIS) Experience
    Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.

KNOWLEDGE, SKILLS, ABILITIES

  • Comprehensive therapeutic area knowledge, clinical development guidelines and directives and regulatory guidelines .
  • Expert knowledge of the key principles of cross functional project management (Time, Quality, Cost).
  • Excellent oral and written communication and presentation skills.
  • Demonstrated leadership and interpersonal skills including the ability to lead, motivate and coordinate cross-functional project teams.
  • Technical and systems competency, such as computer skills, to include effective use of systems and applications such as Microsoft Outlook, Word, Excel and PowerPoint, as well as organization systems (CTMS, Preclarus, Clarity).
  • Proven flexibility and ability to effectively prioritize workload and resources for project team members in a frequently changing environment.
  • Skilled in process improvement and strategic development, especially as it applies to clinical trials, clinical development and project management.
  • Ability to coach, mentor and lead global and/or cross-functional teams with a cultural awareness.
  • Strong financial acumen with an in-depth of knowledge and practical application of budgeting, forecasting and resource management.
  • Excellent customer service, consultation and relationship building skills.
  • Advanced negotiation and marketing skills with ability to influence others and drive results.
  • Excellent judgment, decision making and problem-solving skills and proven ability to apply critical and analytical strategic thinking skills to manage complex/ambiguous situations.
  • Proactive, solutions oriented and skilled at risk identification and management.
  • This position must understand the importance of accurate data, how to use it through acquired technical skills, and how to interpret data to draw conclusions (with support from senior colleagues as needed) so that others can make decisions and problem solve.
  • Responsible for developing the schedules for activities and deliverables for traditional R&D and Medical Projects (all phases: from pre-CS through Phase IV) to an appropriate level of detail that enables the evolving business needs.
  • Expected to recommend changes as opportunities present themselves to improve the efficiency of planning and scheduling of projects to stakeholders.
  • Maintains the system data quality by assuring schedule compliance to established business rules, standards and ways of working along with the accountable Project Manager
  • Responsible for selecting the appropriate Work Packages within the planning system.
  • Build the associated schedules to drive Total Project Cost (TPC) forecast estimates; forecast cost (EPE) and resource (FTE / IPE) associated with integrated plans.
  • Partner with key stakeholders including functional Project Managers, etc. to ensure plan schedule alignment to intended strategy.

Responsibilities:

  • Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
  • Able to work upright and stationary for typical working hours.
  • Ability to use and learn standard office equipment and technology with proficiency.
  • Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
  • May require travel. (Recruiter will provide more details.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Site Engineering / Project Management

Clinical Pharmacy

Graduate

Proficient

1

North Carolina, USA