PM II / Snr PM - Ophthalmology - up to £7,500 sign on bonus

Home-Based, GBR
06 May 2021
05 Jun 2021
Full Time
Experienced (non-manager)
Project Manager II / Snr Project Manager

CNS - Ophthalmology

Competitive salary - Up to £7,500 Sign on Bonus (or currency equivalent ) + Full company benefits

Syneos Health Europe and are seeking a PM II or Snr PM for our CNS Business Unit that can be based from Home or Office throughout Europe - We are looking for PM's who have previouse experience working on ophthalmology studies

Why Syneos Health
• #SyneosHealthLife means we're committed to our Total Self culture - where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person's unique contributions make a difference.

• We believe our success is a direct result of the people who are driving it - you! We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That's why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial.

• We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong.

Job responsibilities

Project Leadership and Delivery:

• Manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance with GCP, relevant SOP's, and regulatory requirements.

• Acts as a primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout according to the Customer's and the Company's contractual agreement.

• Lead project team to ensure quality, timelines and budget management.

• Accountable for the financial performance of each project.

• Coordinate activities and deliverables of all study conduct partners and proactively identify and manage issues.

• Ensure studies are conducted in compliance with GCP, relevant SOP's and regulatory requirements.

• Accountable for all project deliverables for each project assigned.

Documentation and Reporting:

• Responsible for quality and completeness of TMF for assigned projects.

• Accountable for maintenance of study information on a variety of databases and systems.

• Responsible for study management components of inspection readiness for all aspects of the study conduct.

• Oversight for development and implementation of project plans.

• Plan, coordinate and present at internal and external meetings.

• Prepare project management reports for clients and management.

• Developing contingency planning and risk mitigation strategies to ensure successful delivery of study goals.

Business Development:

• Develops strong relationships with current clients to generate new and/or add-on business for the future.

• May participate in bid defense meetings where presented as potential project manager.

Why Syneos Health? 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 25,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most. Evolve in a global company that is always looking for ways to work smarter and more efficiently as the only fully integrated Biopharmaceutical Accelerator. You'll be supported with comprehensive resources based on today's emerging technologies, data, science and knowledge - instead of practices from the past. Teaming with some of the most talented professionals in the industry, you'll gain exposure and work in a dynamic environment to over-deliver and outperform. A career with Syneos Health means your everyday work improves patients' lives around the world.Skills and attributes:
To succeed in this role you will need the following skills/experience:
  • Must have Ophthalmology experience as a PM
  • BA/BS in the life sciences, or equivalent combination of education and experience
  • Previous technical and managerial experience in conducting multi-national and/or local clinical trials in CRO in Oncology - please detail when applying
  • Thorough knowledge of regulatory requirements, drug or device development, and clinical monitoring procedures
  • Presentation, documentation, and interpersonal skills as well as a team-oriented approach

What happens next:
If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity.

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.

"Equal Opportunities Plan. Its objective is to achieve the principle of equality of opportunity in Syneos Health's employment practices ensuring that our workforce is truly representative of each gender and that every employee is respected and is able to work under equal conditions."