European Clinical Project Manager - Uxbridge

Syneos Health
Southall, UK
13 Jun 2019
19 Jun 2019
Contract Type
Full Time
Job Description - European Clinical Project Manager - Uxbridge (19002907)Job Description European Clinical Project Manager - Uxbridge - (19002907) Description European Project
Manager / Clinical Site Manager

Office based - Uxbridge

Sponsor embedded

Here at Syneos Health we are currently recruiting for a European
Project Manager/ Clinical Site Manager to be fully dedicated to our client, a
global pharmaceutical company. This position requires an experienced Clinical
Research professional who is looking to undertake a great opportunity leading
clinical studies and working across the UK, Ireland and the Benelux regions.

Working in a therapeutically aligned environment, with a focus on
Oncology studies, your responsibilities will include:

- Full study ownership from set-up to close-out

- Being the main POC for the investigator to maintaining close
contact with site personnel and Site Monitors

- Identifies potential site issue and suggests resolutions

- Demonstrates understanding of data management activities and performs
clinical data review to monitor data quality and coordinate resolution of
clinical discrepancies

- Provides feedback and status updates to internal stakeholders.
Independently manages activities at the site by providing guidance as required
and by collaborating with other key stakeholders

- Demonstrates an understanding of the overall project goals, the
indication studies and the purpose of the assigned study in meeting the
objectives of the project

- Work closely with other study team members in the coordination
of study activities to meet the appropriate timelines at the site/protocol

- Demonstrates a thorough understanding of all steps in the
clinical research process. Coordinates initial and ongoing training of
Investigators, site personnel, vendors etc, and collaborates with Study
Strategy and Planning when appropriate

- Provides on-going training and mentoring to team members through
a mentoring process using informal and/or formal presentations. Serves as a
resource for colleagues

- Understands how the issues of a single study can impact the
overall project and contributes to establishment of best practices through

You will receive managerial guidance and support at all times from
both the sponsor, and Syneos Health management team. Qualifications Qualifications:

• Bachelor's Degree in allied health fields such as Nursing, Pharmacy, or
Health Science
• Previous clinical trial monitoring experience gained within a CRO or
Pharmaceutical company
• Solid understanding of ICH-GCP guidelines
• Strong project management skills
• Very competent with various forms of technology
• On-site monitoring experience is essential
• Good exposure to Oncology.
• Strong communication skills both written and verbal
• Proven experience of building relationships with site staff

Studies are ran in-house, so candidates with a focus on vendor
management experience only will not be considered.

Fully office based, flexibility to WFH 1 day per week once the
probation period has been completed - 3 months.

The position is offered on a permanent contract with future
opportunities for growth and development within both the sponsor organisation
and Syneos Health.

We have a comprehensive benefits package and offer highly
competitive remuneration.

To find out more about our company and search and apply for other
open jobs please visit our website

Join a game-changing company that is reinventing the way therapies
are developed and commercialized. Created through the merger of two industry
leading companies, INC Research and inVentiv Health, we bring together more
than 22,000 clinical and commercial minds to create a better, smarter, faster
way to get biopharmaceutical therapies into the hands of patients who need them
most. #LI-AB2 Primary Location: Europe - GBR-Client-BasedJob: Clinical Project ManagementSchedule: Full-timeTravel: NoEmployee Status: Regular

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