Why Patients Need YouControlling risk and achieving planned study start-up timelines procurement processes is needed to getting our next meaningful medication to market to help those in need. Your role is critical to getting our medicines in the hands of the people who need them most, faster and more efficiently than ever before.What You Will AchieveYou will negotiate contract terms and budgets following processes designed to manage risk to Pfizer and obtain desired study start-up timelines.As an ICL1 , you provide guidance to operational teams for managing projects. Your planning skills will help in preparing accurate timelines for site activation and your experience will help to find ways to improve upon processes. Through your comprehensive knowledge of principles, concepts and theories of the discipline, you will also work towards advancing new concepts and methodologies. You will be able to take a leadership role to facilitate agreements between different teams including monitoring and influencing the progress of other ICL assigned to your study.How You Will Achieve It
Exercise good judgment in balancing the risks for Pfizer in making budget and contractual decisions against the impacts to Pfizer clinical trial timelines.
Follow processes to develop, negotiate, track and execute global clinical study agreements with institutions and investigators participating in sponsored clinical trials.
Work with partners to develop and oversee the global site budget process.
Work with clinical trial sites and directly negotiate cost, business and contractual terms and conditions with investigators/institutions, making changes to contract templates within the Legal division approved parameters.
Lead and develop relationships with key investigational sites and Site Management Organizations across the contracting and budgeting interface.
Lead study level site contracting activities, direct other ICL and act as primary study point of contract for site contracting issues and timelines on assigned studies.
Partner with Legal and other divisions to manage escalations in the site budgeting and contracting space.
Partner with Legal, Finance, CRO and other divisions to identify and implement areas of improvement in the site contracting space.
Demonstrate knowledge of the principles, concepts and theories in applicable business disciplines.
Collaborate with invoicing specialists and/or invoice service provider to ensure alignment with Investigative Site contracting and compensation requirements.
Apply acquired job skills and procedures to complete substantive assignments, projects and tasks of moderate scope and complexity in applicable discipline.
Contribute to design, development and implementation of major business initiatives or special projects. Applies technical skills and discipline knowledge to contribute to the achievement of business objectives at the Functional Line level.
QualificationsMust-Have
5+ years of experience in clinical development operations or clinical trial outsourcing and a bachelor's degree.
Experience in drafting and negotiating of Clinical Trial Agreements with clinical trial sites in a global operation.
Experience with clinical study budgets and contracting negotiation principles, practices, processes, and activities.
Balance of general business, compliance, finance, legal, and drug development experience.
Precise communications and presentation skills.
Ability to plan, identify and mitigate risks to site contacting timelines.
Demonstrated ability to lead by influence rather than positional power to accomplish critical deliverables.
Demonstrated success in working in a highly matrix-based organization.
Nice-to-Have
2+ years of experience in clinical development operations or clinical trial outsourcing and a US Juris Doctorate or equivalent legal degree.
PHYSICAL/MENTAL REQUIREMENTS
None
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
None
Other Job Details:
Last Date to Apply: 205 AUGUST 2024
Eligible for Employee Referral Bonus.
Work Location Assignment:Remote - Field BasedThe annual base salary for this position ranges from $93,500.00 to $155,900.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 12.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.Relocation assistance may be available based on business needs and/or eligibility.Sunshine ActPfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.EEO & Employment EligibilityPfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.Global Procurement
