Move to the Uk as A Project Manager – Visa Sponsorship.

If you’re in search of a Visa-sponsored job, we’ve got you covered. This job opportunity provides Visa Sponsorship, so please carefully review the details below:

 

About the Role

The Project Manager will be based at the Centre for Clinical Vaccinology and Tropical Medicine and will oversee the management of clinical trials and programs. Key responsibilities include sponsor/CTRG liaison, project assessment, ethics and regulatory submissions, resource procurement and planning, project implementation, milestone tracking, adherence to quality standards, SOPs, ICH-GCP, and more. The role also involves managing communication between the project team, sponsor, contract, and financial management.

 

Roles & Responsibilities

  • Project coordination and management
  • Manage various projects, commercial or publicly funded.
  • Develop, manage, and execute project plans and timelines.
  • Support the project team in completing assignments.
  • Ensure compliance with protocols and administrative requirements.
  • Monitor project progress, identify issues, and rectify problems.
  • Work with Quality Assurance Manager on audit processes.
  • Collaborate with Principal Investigator for project targets.
  • Proactively manage projects and anticipate and resolve problems.
  • Support project-related meetings and groups.
  • Ensure efficient data management in collaboration with the IT Manager.
  • Handle ethics applications, regulatory submissions, and NHS Research and Development.
  • Facilitate discussion between Sponsor and Principal Investigators.
  • Maintain financial records and oversee expenses.
  • Ensure projects are completed on time and within budget.
  • Complete administrative closeout procedures and archive projects.
  • Communications and networking
  • Serve as the primary contact for the Sponsor as needed.
  • Coordinate internal and external project communication.
  • Prepare and publish data, reports, and information.
  • Liaise with various departments for effective working relationships.
  • Facilitate information sharing and communication within the team.
  • Represent Project Management at meetings.
  • Prepare and submit project plans and reports to the Sponsor.
  • Provide regular information and updates to trial participants and sponsors.
  • Supporting research team
  • Identify grant opportunities for researchers.
  • Address the training needs of research staff.
  • Assist the Principal Investigator in grant applications.
  • Evaluate project activities and integrate lessons learned into future proposals.
  • Assist with recruitment, training, and supervision of team members.
  • Report resource and training needs to Line Managers.

Eligibility Requirements

Essential:

  • Degree in life science or health-related subject or relevant clinical trial experience.
  • Knowledge of GDPR, GCP, Research Governance, and regulatory frameworks.
  • Understanding of the UK regulatory and governance environment.
  • Project management experience in a clinical setting.
  • Proficiency in report writing and clear presentation of complex information.
  • Experience in creating study costings.
  • Strong organizational, communication, and interpersonal skills.
  • Initiative, problem-solving ability, and attention to detail.
  • Ability to work independently and as part of a team.

Desirable:

  • Previous clinical experience.
  • Effective negotiation and facilitation skills.
  • Audit experience.
  • Experience in higher education, industry, or NHS interface.
  • Information technology skills, especially Microsoft Office.

Application Process

You’ll need to submit a CV and Supporting Statement as part of your online application, including a cover letter that addresses how you meet each selection criteria in the job description. For more information on writing an effective Supporting Statement, visit this link.

To Apply, Click Here.

 

Note

Only online applications received before 12.00 midday on 21/11/2023 will be considered. Interviews will be held as soon as possible thereafter.

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