Clinical Project Manager ll

As a Clinical Trial Project Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

• The Clinical Trial Manager (CTM) is accountable for achieving successful delivery of clinical activities at the project level by meeting internal and external contractually agreed client and regulatory requirements according to time, quality/scope and budget constraints. The Clinical Trial Manager (CTM) leads and directs cross functional teams and understands/manages client expectations. In addition, the Clinical Trial Manager (CTM) proactively identifies, resolves/mitigates and escalates risks and/or issues. Depending on the business unit the descripted accountabilities may or
  may not apply.

   

  • Daily Management of a Trials
  • POC for sponsor, sites and CRAs
  • Study Tracking and Monitoring trip report review

   

  Provides Project Oversight and Leadership for Clinical Deliverables:

  Leads and manages the start-up and clinical teams

  Plans and leads execution of the day to day activities for the monitoring of a clinical study

  and communicates consistently with the clinical team providing project objectives, expectations and

  status updates. Works with the team to set priorities

  Takes the initiative to make things happen and leads and supports the relevant staff ( this may

  include but is not limited by Country Start Up Specialist (CSS), Global Regulatory Affairs Lead

  (GRAL), Local Regulatory Affairs Lead (LRAL) and In-House Clinical Research Associate (IHCRA)) to

  ensure the successful activation of trial sites according to time, quality/scope and budget

  parameters

  Motivates the clinical team

  Ensures effective communication plans are place for the clinical team Ensures effective escalation

  plans are in place for the clinical team

  Works with the Project Manager (PM) to facilitate cross functional team and sponsor communication

  for proactive, study-wide problem solving regarding study progress and trial issues during the

  study

  Monitors the quality of clinical deliverables and addresses quality issues with the appropriate

  team member

   

   

  Oversees the GRAL, LRAL and IHCRA to ensure that all non-safety periodic updates, progress reports and

  renewals and/or end of study notifications are performed in accordance with the trial protocol, local regulations,

  ICH-GCP and any other processes or procedures governing the clinical trial.

  Identifies metrics and trends across team members, countries, regions and uses the information to

  promote improvement in quality and consistency of execution.

  Collaborates with Quality Assurance (QA) to identify sites needing corrective and preventative action plans,

  responds completely and accurately to audit reports, provides team with project-specific audit process to ensure

  adequate preparations/reviews of all audit responses prior to submission to internal clinical review team/QA and

  then Sponsor Organizes project specific compliance plans for key processes, tools and systems

  Reviews filing of Essential Documents in the electronic Trial Master File to ensure sponsor and investigator

  obligations are being met and are in compliance with applicable local regulatory requirements and ICH guidelines

  Project Finance

  Provides Time Entry Guidelines to the relevant study team members in adherence with project scope and budget;

  monitor burn rates, escalating issues with potential solutions to the Project Manager (PM).

  Forecasts units and hours and generic resources for the start-up and monitoring activities, determines worked units

  and hours, analyzing forecasted and worked activities to ensure adherence to contract and budget

  Ensures that forecasted units are achieved as planned and within the budgeted FTE

  Identifies out-of-scope tasks from clinical team and escalates as required

  Ensures no out-scope tasks be conducted without the required evidence of agreement from the client or approval

  by the relevant PRA staff.

  Customer Relations (Internal & External)

  Interfaces with other Functional Leads, vendors and client as required to ensure clinical monitoring outcomes are

  achieved

  Serves as primary liaison for clinical monitoring issues, interacting with clients, vendors and other PRA functional

  areas, escalating as required

  Participates in client meetings, assisting with presentations as required

  Contributes to Business Development activities

Education: 

• Bachelors Degree in health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required.

Experince requried: 

• 3-5 years of clinical research project management experience required

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

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, color, 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.