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Singapore

Clinical Trial Manager- FSP

Parexel
$60,350 - $76,417 a year
Singapore
2 days ago

Primary Location: Singapore
Job ID R0000035100

Category Clinical Trials

ABOUT THIS ROLE

Key Accountabilities:

Client Liaison:

  • Effectively communicate with internal and external customers as well as third party vendors;
  • Prioritize effectively and respond to urgent requests within team or from sponsor.

Project Initiation & Planning:

  • Manage study start-up activities
  • Provide input to project tools, PM plan, Central File Maintenance Plan
  • Provide input to the format and content for sponsor reports
  • Provide input to and oversight of site selection strategy plan
  • Develop site selection and monitoring plans for the team
  • Review and provide input into patient recruitment plan and retention plan
  • Ensure all team members have access to tools and documents
  • Establish efficient / effective working relationships with other functional Leaders and coordinators across geographies within a given program
  • Develop study plans, tools and forms.

Project Implementation, Control & Evaluation:

  • Provide leadership and direction to project team members
  • Identify, organize and deliver (where appropriate) study specific training in collaboration with Project Leader and Project Specialists
  • Evaluate and identify resourcing needs and continuously monitor the use of resources over project life cycle
  • Provide productivity targets to project team members
  • Provide performance feedback on team members as appropriate
  • Address identified and escalated site issues and drive to closure
  • Early recognize areas of potential problems and provide input to contingency plans
  • Monitor study timelines, patient recruitment, retention and data cleaning to ensure successful outcome of the project
  • Oversee maintenance and quality check of Central Files
  • Maintain and assure quality of work generated and escalate and follow up as appropriate
  • Ensure appropriate handover between project team members with support from Clinical Operations Managers
  • Implement and instigate process improvements within the project
  • Provide input to the Revenue Recognition forecast
  • Identify changes in scope and liaise with Project Leader
  • May be required to conduct site visits as per client or project demands
  • Participate in client, investigator and team meetings
  • Prepare, participate in and follow up on audits / inspections
  • Participate in all required applicable trainings

Project Close-out:

  • Collaborate with project team (e.g. Project Leader and Data Operations Leader) on database lock activities
  • Together with Project Leader ensure all administrative closeout procedures are completed according to Project Close-out Checklist
  • Together with Project Leader ensure project is archived and all documentation returned to the client as specified by the contract
  • Participate in end of study meeting and give input to lessons learned information and feedback relevant information into the relevant functions

Operational:

  • Maintain a working knowledge and ensure compliance with applicable ICH-GCP Guidelines, local regulatory requirements and PAREXEL WSOPs, SOPs, Operational Guidelines, Work Instructions and study specific procedure
  • Complete routine administrative tasks in a timely manner (e.g. timesheets, metrics, office and travel expense claims)

Skills:
Leadership skills that include:

  • Ability to lead a virtual team across locations and cultures
  • Carefully weigh the priority of project tasks and direct team accordingly
  • Enlist the support of team members in meeting goals
  • Ability to negotiate and influence with diplomacy in order to achieve results
  • Ability to make decisions even in ambiguous situations to achieve project timelines and quality
  • Ability to proactively identify and solve problems by using a logical, systematic approach
  • Ability to conduct root cause analysis in business problem solving and process improvement development
  • Strong customer focus, ability to interact professionally within a client organization
  • Ability to manage multiple and varied tasks with enthusiasm, prioritize workload with attention to detail
  • Effective time management in order to meet daily metrics or team objectives

Personal skills that include:

  • Ability to take initiative and work independently
  • Ability to successfully work in a team environment
  • Sense of urgency in completing assigned tasks
  • Commitment to high quality work and respective consistent performance
  • Excellent interpersonal, oral and written communication skills
  • Ability to gain trust and confidence with a client as well as within PAREXEL
  • Good learning ability
  • Action oriented
  • Excellent presentation skills
  • Good consulting skills
  • A flexible attitude with respect to assignments and new learning
  • Ability to travel as required

Business / operational skills that include:

  • Customer focus
  • Commitment to delivery and quality
  • Proactive issue identification and resolution
  • Provision of win-win solutions to problems
  • In-depth understanding and experience in the clinical trial process and understanding of all aspects of project life cycle
  • Knowledge of SOPs/guidelines, ICH-GCP and other applicable local and international regulations
  • Ability to become proficient with PAREXEL systems
  • Proficient computer and internet skills including knowledge of MS-Office products such as Excel, Word, Power Point, Outlook, WebEx


Knowledge and Experience:

  • Strong command of written and spoken English language, local language proficiency as required
  • Proven clinical experience or management experience in healthcare, clinical research, or contract research organization
  • Substantial experience in clinical research including relevant experience as a team Leader in Clinical functions or proven experience in coordinating clinical trials. Relevant Work experience in clinical research
  • Experience in Coordination of Clinical Trials – Preferably relevant working experience as an Associate Clinical Operations Leader or proven experience in a similar role
  • Individuals should have a strong understanding of the cross functional activities


Education:

  • Degree in a life science, nursing qualification or relevant clinical and or clinical management experience
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