Empleos actuales relacionados con Site Contracts Template Specialist, Clinical Development - Madrid - Pfizer


  • Madrid, España Cmed A tiempo completo

    Cmed occupies a unique position in the clinical research industry, not only as a CRO expert in the operational delivery of clinical trials in complex disease areas including oncology, immuno-oncology, and cell therapy, but also as a developer of its own cutting-edge technologies for managing clinical data. encapsia® is our ultramodern, innovative and game...


  • Madrid, España Caidya A tiempo completo

    **Job Title**: Associate Director, Clinical Site Contracts **Job Location**: Europe - Remote **Job Overview**: The Associate Director, Clinical Contracts will manage the Clinical Contracts (Legal) team to provide the leadership, support, and guidance to successfully lead a global, company-wide Clinical Contracts team. This position requires an effective...

  • Contracts Manager

    hace 7 meses


    Madrid, España Caidya A tiempo completo

    **Job Title: Contracts Manager** **Job Location**: Madrid, Spain (home-based position, any location in mainland Spain considered)**Job Overview**: The Contracts Manager (CM) will oversee the cross-functional execution of Clinical Contracts to ensure consistency and quality while identifying and solving any issues that potentially would delay the negotiation...


  • Madrid, España Cmed A tiempo completo

    The Aixial Group is an International Contract Research Organization (CRO), a member of the ALTEN Group, providing complex services in clinical trials (phase I-IV) and non-interventional studies. Our offices are located in France, Belgium, Switzerland, Germany, Denmark, Sweden, UK, Romania, US, India and Czech Republic. Through Cmed (a part of the Aixial...

  • Contracts Manager

    hace 7 meses


    Madrid, España Caidya A tiempo completo

    Contracts Manager (CM) - home-based position in Spain. Caidya is seeking a Contracts Manager (CM) to join our team. As a Contracts Manager, you will play a critical role in overseeing the cross-functional execution of Clinical Contracts, ensuring consistency and quality throughout the process. Your responsibilities will include supporting the study Project...


  • Madrid, Madrid, España Medpace A tiempo completo

    Job SummaryMedpace is a full-service clinical contract research organization (CRO) with a rapidly growing European presence. We are seeking a highly skilled Clinical Operations Manager - Site Contract Specialist to join our team in Madrid.This role will play a key part in the study start-up and clinical trial management processes at Medpace, working closely...


  • Madrid, Madrid, España Ora A tiempo completo

    About OraOra is a leading full-service ophthalmic drug and device development firm, guiding clients across all phases of clinical research to efficiently bring new products and therapies to market.Our MissionWe prioritize kindness, operational excellence, and cultivating joy in our work, while maintaining scientific rigor. Our team has helped earn over 85...

  • Contract Specialist

    hace 2 meses


    Madrid, España Ora A tiempo completo

    .POSITION TITLE: Contract SpecialistDEPARTMENT: Ora EuropeLOCATION: Remote in UK, Spain, Italy or PolandOra Values the Daily Practice of ...Prioritizing Kindness * Operational Excellence * Cultivating Joy * Scientific Rigor----------------------------------------At Ora, we are building the future of ophthalmic clinical research. As the world's leading...


  • Madrid, España Ergomed A tiempo completo

    Company Description Ergomed is a rapidly growing global clinical research company. We perform clinical trials for rare and complex diseases. Ergomed Plc is a public company on the London stock exchange. The company boasted 40% growth in its revenues in its last report. This success is due to the hard work of our highly skilled employees and our subsequent...


  • Madrid, España Resourcing Life Science A tiempo completo

    Company DescriptionOur client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Clinical Contract Specialist office based in Spain.Job OverviewPrepare & negotiate site...


  • Madrid, España Ergomed A tiempo completo

    Company Description Ergomed PLC is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you...


  • Madrid, España Syneos Health, Inc. A tiempo completo

    .CTA / Site Contract Specialist. BCN or MAD. Sponsor dedicatedUpdated: November 16, 2024Location: Spain-Europe - ESP-Home-Based (Madrid)Job ID:24006274Syneos 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...


  • Madrid, Madrid, España Ora A tiempo completo

    Company OverviewOra, a leading full-service ophthalmic drug and device development firm, guides clients across all phases of clinical research to efficiently bring new products and therapies to market. With 45 years of experience, Ora has helped earn over 85 new product approvals through its expert teams and refined methodologies.About the RoleThe Clinical...


  • Madrid, España Syneos Health, Inc. A tiempo completo

    .CTA / Site Contract Specialist. BCN or MAD. Sponsor dedicated Updated: November 16, 2024Location: Spain-Europe - ESP-Home-Based (Madrid)Job ID: 24006274Syneos 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...

  • Site Contracts Associate

    hace 3 semanas


    Madrid, España Parexel International A tiempo completo

    Parexel is in the business of improving the world's health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep...

  • Ad Site Contracts

    hace 2 días


    Madrid, España Thermo Fisher Scientific A tiempo completo

    At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...


  • Madrid, España Pfizer A tiempo completo

    JOB SUMMARY Creating value though site contracting is keeping our products in production and our innovators innovating. Whether you are part of negotiating contracts or budgets, planning site contracts milestones, 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. The...


  • Madrid, España Fortrea A tiempo completo

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • Site Contracts Associate

    hace 3 semanas


    Madrid, España Parexel International A tiempo completo

    Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep...

  • Site Contracts Associate

    hace 3 semanas


    Madrid, España Parexel International A tiempo completo

    Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep...

Site Contracts Template Specialist, Clinical Development

hace 6 meses


Madrid, España Pfizer A tiempo completo

Must have experience within Biopharmaceutical Industry

ROLE SUMMARY

The site contracts template specialist is responsible for identifying, prioritizing opportunities, and achieving and maintaining appropriate inventory of site contract templates. This role is responsible for revising global, country and site-specific templates to align changing external (legal, regulatory, financial) and internal requirements. This role requires drafting, reviewing and communicating changes to site contract templates and maintaining the template library.

ROLE RESPONSIBILITIES

Is divisional subject matter expert for all country and site template updates for Pfizer Research & Development and Pfizer Oncology Divisions. Maintains strong business awareness, evaluating current and possible future policies, practices (including governmental acts and policies), trends, technology, and information potentially affecting Investigative Site Contracting. Recommends changes to templates based on knowledge and experience. Responsible for collaborating with Pfizer Legal to ensure Investigative Site contracting templates are maintained and continuously improved. Manages the introduction of revised templates by gaining appropriate approvals and by efficiently communicating changes to all stakeholders, including those outside the site contracting group. Updates contract template guidance and repository to support contract template changes. Accountable for ensuring training is delivered and documented to site contracting professionals around Investigative Site Contracting policies, templates and standards. This role also involves direct negotiation or oversight of other site contracting professionals in negotiation and execution of assigned contracts. 

BASIC QUALIFICATIONS

 7+ years of experience in clinical development operations or clinical trial outsourcing and a bachelor’s degree or equivalent. Experience in working with limited supervision to achieve business goals. Experience with contracts and negotiation principles, practices, processes, and activities is essential. Balance of general business, compliance, finance, legal, and drug development or legal / compliance experience in a regulated industry is essential. Strong and precise communications and presentation skills essential to success. Record of achievement and delivery against personal goals. Demonstrated ability to lead by influence rather than positional power to accomplish critical deliverables. Demonstrated success in working in a highly matrix-based organization.

PREFERRED QUALIFICATIONS

5+ years of experience in clinical development operations or clinical trial outsourcing with a master’s degree. 2+ years of experience in clinical development operations or clinical trial outsourcing with a Juris Doctorate (or equivalent). Expertise in drafting and negotiating of Clinical Trial Agreements with clinical trial sites in a global operation.


Work Lo

#LI-PFE

#LI-Remote

The 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 Act

Pfizer 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 Eligibility

Pfizer 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