Farmacéutico/A Adjunto/A - Fines De Semana- Fuenlabrada

Farmacias Trebol; Fuenlabrada; Presencial; EUR 33.000 - 55.000; Jornada completa

Descripción de la vacante

Stryker Madrid is seeking a Senior Global Trial Manager to lead cross-border clinical delivery for large multi-regional studies, ensuring compliance with ICH-GCP, SOPs, and project plans.

You will manage risk, coordinate with internal and external stakeholders, mentor teams, and contribute to study delivery strategy while aligning with regional RAQA activities.

Formación

• Bachelor's degree in health care or other scientific discipline.
• Experience with regulatory requirements (GCP/ICH).
• Ability to manage multiple projects and stakeholders.

Responsabilidades

• Ensure clinical delivery in compliance with regulatory requirements and SOPs.
• Meet project clinical targets and manage risks throughout the lifecycle.
• Coordinate with internal and external stakeholders to ensure timely delivery.
• Lead and mentor clinical teams to achieve milestones.
• Prepare and communicate project status and issues to senior management.

Conocimientos

Project management

GCP/ICH knowledge

Stakeholder management

Regulatory communications

MS Office

Educación

Bachelor's degree in health care or other scientific discipline

Herramientas

CTMS

Microsoft Office

Descripción del empleo

Position Summary
Develops and applies intermediate knowledge and understanding of the PMS /RA / QA PMS frameworks, legislative requirements, processes and procedures in the EMEA distribution organisation.

Key Activities & Accountabilities

• Customised according to PMS/ RA / QA / pillars.
• Executes PMS/ RA / QA / activities in line with defined procedures and processes.
• Collects, organises and maintains files on local, regional, and global RAQA intelligence.
• Identifies the need for new regulatory procedures, SOPs, and participates in development and implementation.
• Identifies opportunities for continuous improvement and supports those activities across RAQA.
• Performs based on established targets, KPIs and objectives for RAQA.
• Provides support to EMEA / Country RAQA teams as appropriate.

Education

BSc degree in relevant field.

Experience

0-2 years' experience.

Knowledge/Competencies

• Project management and time management skills, writing, coordination, and execution of more complex PMS/ RA / QA / items.
• Coordinate and support and lead technical and scientific PMS/ RA / QA / activities.
• With minimal supervision, performs work that is varied and that may be somewhat difficult in character, conferring with superiors on unusual matters.
• Undertaking assignments that are broad in nature, requiring originality and ingenuity.
• Ability to take limited unreviewed action or decisions.
• Clearly conveys information to peers, supervisors, and other stakeholders across the EMEA organisation, Design Divisions and third‑party distributors.
• Prepares for meetings with regulatory agencies, internal and external audits and other stakeholders, with minimal support.
• Assists in the preparation of briefings and other information documents.
• Communicates information and advises on PMS/ RA / QA / requirements to other departments and business units.
• Engages in communication with regulators and other key stakeholders on routine and complex matters with minimal supervision.
• Creates clarity and direction amid complexity and develops solutions for self, colleagues, and the organisation.
• Seeks out diverse ideas, opinions and insights, and applies them in the workplace.
• Connects and relates well with people who think and act differently than oneself.
• Embraces scrutiny and accepts feedback as opportunity to learn and improve.
• Preparation of PMS/ RA / QA / metrics for reporting purposes.
• High attention to detail and process consciousness.
• Strong IT skills, including Microsoft Office.
• Fluent in English (+ local language where applicable).

Spain Pay Ranges:

• Spain : 32.900 - 54.700 EUR Annual

At Stryker, we believe transparency helps candidates make confident decisions about their next career step. Compensation is an important part of that process and we want to be clear about how pay is determined. The compensation information posted for this role may be presented as a salary range or a fixed amount depending on the role. In addition to base salary, this role may be eligible for incentive compensation (such as bonus and/or commissions where applicable), along with Stryker's comprehensive benefits package.

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

Locations and Work Arrangements

• Madrid, Spain
• Reading, Berkshire, United Kingdom
• Barcelona, Spain

Contract Type: Full time

Job Overview

Senior Global Trial Managers (SGTMs) are an integral part of clinical trial delivery, leading and working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The SGTM is a member of the core project team responsible for clinical delivery of large, multi‑regional studies to meet contractual requirements and in accordance with (Standard Operating Procedures) SOPs, policies and practices. SGTMs ensure clinical delivery to customers by leading clinical teams and partnering with other functional teams to ensure projects meet delivery requirements at all times.

Responsibilities

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonisation (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).
• Accountable for meeting projects' Clinical targets.
• Contribute to the development of the project risk mitigation plan. Manage clinical risks through the project lifecycle.
• Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.
• Manage clinical aspects of Project. Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against Study work plan (SWP) and identify additional service opportunities or out of scope work to be manage on a Change in Scope (CIS) process.
• Work as the primary Point of contact for the customer project manager.
• Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.
• Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.
• Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high‑quality operational plans and guidance and project related trainings.
• Conduct regular team meetings and communicate appropriately to achieve objectives.
• Support professional development by providing feedback to clinical team line managers on performance relative to project tasks to support professional development.
• Adopt corporate initiatives and changes and serve as a change advocate when necessary.
• May contribute to the development of the clinical delivery strategy for business proposals. Participate in bid defense preparations and meetings. Develop and present Clinical Operation plan in partnership with Business Development and Project Leadership.
• May mentor and coach new peers as they assimilate into this role.
• May attend site visits as applicable in support of project delivery.

Requirements

• Typically requires 3 - 5 years of prior relevant experience.
• Bachelor's degree in health care or other scientific discipline required.
• Requires 7 years clinical research/monitoring experience or equivalent combination of education, training and experience.
• Requires consolidated knowledge and understanding of Project management practices and terminology.
• Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Requires broad protocol knowledge and therapeutic knowledge.
• Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.
• Requires understanding of project finances to oversee the clinical/monitoring budget and changes to scope.

This position is not eligible for UK VISA Sponsorship

Salary

The potential base pay range for this role, when annualized, is 217.800,00 - 404.600,00 PLN zł. The actual base pay offered may vary based on a number of factors including job‑related qualifications such as knowledge, skills, education and experience; location; and/or schedule (full or part‑time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at .

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi‑talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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