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Site Id Lead Jobs

Company

Syneos Health

Address Canada
Employment type FULL_TIME
Salary
Category Research Services,Biotechnology Research,Pharmaceutical Manufacturing
Expires 2023-06-14
Posted at 11 months ago
Job Description
Description
Site Identification Lead
Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers achieve their objectives.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
  • 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.
  • We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
  • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
Job Responsibilities
  • Project-specific financial management including, but not limited to:
  • Support the PL and contract analyst in the generation of out of scope estimates for change in scope projects
  • Leads the technical and operational site identification aspects of global projects including tracking and weekly reporting of project deliverables to Site ID Manager, Internal Project Team, and Sponsor. Attends project team and client meetings to represent the Site Identification team and provide updates on site identification feasibility status.
  • Develops the Site Identification plan (Site ID checklist), with input from the Sponsor and Project Lead (PL), and by understanding the project's strategy via the feasibility workbook and Proposal document. This also includes negotiation and finalization of supporting documents such as the Confidential Disclosure Agreement (CDA) template and CDA playbook, Site ID Cover Letters, etc.
  • Proactive in identifying scope creep & communicating to Site ID Manager & PL.
  • Ability to understand and translate protocol requirements to develop the ideal site profile, in collaboration with Sponsor and key cross-functional leads. Mine relevant databases, epidemiology resources, available literature resources, etc. to identify the best suited sites for the project and proactively advocate for inclusion of strategic relationship sites with sponsor and project team as appropriate.
  • Communicating changes to resource requirements (change in scope) to LM’s and central resourcing team
  • Drafts the potential investigator feasibility questionnaire template, with input from Project Lead (PL), Medical Monitor, Clinical Lead, etc.
  • Ensures site identification team is updating and maintaining all project-required systems (investigator databases, trial master file, study repository, and any other project-specific tracking tool) per company and/or sponsor SOPs, processes and work instructions.
  • Analyzes survey data and produces final site identification deliverable including site identification recommendations to PL and/or sponsor. As part of final deliverable, may develop assumptions for enrolment modelling and predictive analytics (e.g. for Monte Carlo Simulation).
  • Able to train and mentor site identification project team members on project protocol, study-specific requirements, and the site identification process. This includes management of performance and quality of work to meet project goals.
  • Responsible for site identification related resource management for studies including, but not limited to:
  • Forecast units
  • Provide oversight to team of local country resources for the conduct of site identification activities.
  • Requesting country level resources to support projects based on scope & budget
  • Responsible for revenue recognition of assigned projects
  • Understanding costing tool & translation into activities and hours
  • Responsible for obtaining final site list from PL and ensuring sites are notified of non-selection decision based on results of initial site level feasibility assessment.
Qualifications
What we’re looking for
  • Experience working in a pharmaceutical, biotech, contract research organization or clinical research site
  • BA/BS in the biological sciences or related discipline in the natural sciences/health care field (e.g. RN)
  • Ability to multitask under tight deadlines on several projects with specific and unique requirements, while providing attention to detail and high quality work
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, database applications), email, and internet
  • Ability to be flexible, adapt to change, work independently, as well as work as part of a team in a matrix environment
  • Excellent verbal, written, communication and time management skills
  • Strong presentation skills, interpersonal skills, as well as a team oriented approach.
  • Strong study-level and department-level operational experience with a willingness to challenge oneself to meet study, department, and company goals
Get to know Syneos Health
  • Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health
Additional Information
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 . 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. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.