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Site Grant Management - EMEA any country (experience in building budget for sites, pricing, negotiation)

Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 
Panama, Pennsylvania (USA), United States

Offer summary

Qualifications:

BS degree in life sciences or health-related field, Extensive experience in CRO/pharmaceutical industry, Thorough knowledge of drug development regulations, Proficient in MS Office and other tools, Ability to handle multiple tasks in dynamic environment.

Key responsabilities:

  • Establish and update training materials for budgeting team
  • Propose budget solutions and ensure deliverables are met
  • Develop and maintain investigator grant budget estimates
  • Collaborate with internal and external stakeholders on budget templates
  • Identify opportunities for continuous process improvement
Syneos Health logo
Syneos Health Biotech: Biology + Technology Large https://www.syneoshealth.com/
10001 Employees
See more Syneos Health offers

Job description

Description

Principal, Site Grant Management

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

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 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.
  • 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 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

  • Establishes, maintains and updates training material for investigator budget team and site contract negotiators.
  • Actively participates in higher-level discussions about overall company goals, functional objectives in the Business Unit (BU), and specific project aims.
  • Serves as subject matter expert equipped to help resolve global site budgeting issues, and escalation point within the Company for internal customers to seek assistance.
  • Proposes site budgeting solutions to issues that may arise during a project or contract/budget life cycle to enhance negotiation strategy and ensure deliverables are met.
  • Establishes project strategies around investigator budget template development and/or budget negotiation parameters to reflect sponsor's specifications, communications and required processes. Initiates and introduces creative ideas and solutions.
  • Develops detailed investigator grant budget estimates and country budget templates according to protocol specifications through currently available software package/resources.
  • Updates detailed investigator grant budget estimates and country budget templates according to protocol amendment specifications through currently available software package/resources.
  • Works closely with internal stakeholders to draft, collaborate with Sponsor and harmonize investigator budget templates, investigator budget parameters and payment terms within Company processes.
  • Ensures investigator budget templates are drafted and updated taking into consideration fair market value and key operational aspects indicated in the relevant operational documents (e.g. protocol, Integrated Site Activation and Maintenance Plan, etc.), as well as in the customer agreement documents at a project and organizational level.
  • Establishes strong working relationships and collaboration with Sponsor to ensure site budget templates fit into the global strategy set for the program.
  • Validates investigator grant budget estimates against available internal and external benchmarking data.
  • Identifies possible investigator budget or process operational risk and proactively works to provide solutions.
  • Establishes strong working relationships with customer and internal project teams.
  • Escalates deviations to senior management and is equipped to resolve issues with Quality Assurance.
  • Creates and maintains document status reports, and updates department tools/systems and team members on a regular basis; ensures appropriate documentation is maintained.
  • Collaborates with internal and external legal, finance and clinical operations departments, including communicating and explaining legal and budgetary issues.
  • Researches, compiles and creates necessary information as required in support of obtaining fair market value and developing investigator budget templates.
  • Identifies best practices, investigates root causes of fundamental issues and problems for projects and recommends solutions. Recognizes and develops opportunities for continuous process improvement within investigator budget template development, which lead to greater efficiencies and/or leading best practices.
  • Trains and mentors less experienced staff members on department Standard Operating Procedures (SOPs), processes, tools and templates and ensures quality of teamwork products.
  • Represents the Company at professional meetings or seminars.
  • May support BU and organization through help desk and other defined pathways to resolve and deescalate issues.
  • May identify and lead internal team training and/or process improvement initiatives.
  • Participates in business development presentations as a subject matter expert in budget development and Fair Market Value (FMV) within the Company.
  • Performs other work-related duties as assigned. Minimal travel may be required (up to 25%).

Qualifications

What we’re looking for

  • BS degree in life sciences, a health related field, or equivalent combination of education and experience.
  • Extensive experience in a CRO/pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience.
  • Thorough knowledge of applicable regulations, drug development and clinical project management procedures.
  • Excellent presentation, documentation and interpersonal skills. Proficient in MS Office (Word, Excel and PowerPoint), MS Project, outlook and Internet.
  • Ability to handle multiple tasks to meet deadlines, delivering high quality work in a dynamic environment.
  • Above-average attention to detail, effective oral/written communication skills along with the ability to work independently to meet deadlines.
  • Excellent leadership skills; ability to teach/mentor team members.
  • Ability to coach employees to reach performance objectives.
  • Strong background in issue resolution, meeting customer deliverables and driving best practices at organization or customer portfolio level.

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 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. 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.

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Biotech: Biology + Technology
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Time Management
  • Budgeting
  • Microsoft Office
  • Leadership
  • Negotiation
  • Non-Verbal Communication
  • Detail Oriented
  • Social Skills
  • Coaching

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