Clinical Trial Posting Manager at Bayer AG - USA

Santanyí, Balearic Islands, Spain -

Full Time

Start Date

Immediate

Expiry Date

17 Jul, 26

Salary

0.0

Posted On

18 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical trial management, Regulatory compliance, Quality assurance, Project management, Data disclosure, Drug development, Stakeholder management, Communication skills, Agile methodology, Problem solving, Regulatory affairs, ICH/GCP regulations, IT systems proficiency

Industry

Chemical Manufacturing

Description

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice. Clinical Trial Posting Manager Job Description Summary: Develops or contributes to the development of the organization's products once human trials begin. Participates in international product teams to define and implement development policy and programs that best support the product strategy and future positioning of the organization. Purpose: Operational public disclosure of clinical trial information into clinical trial registries and posting of clinical trial result summaries on company owned and public international websites based on internal rules and external guidelines, obligations, and legislations for the entire Bayer product portfolio, including regular updates and maintenance of the disclosed information according to internal and external requirements Contribute to the development and continuous update of Bayer's disclosure processes for clinical trial information based on cross functional internal requirements and the rapidly changing external legal and regulatory requirements, industry commitments and obligations Disclose information on Bayer's Clinical Trials at high level quality by fully complying to the related Quality Assurance processes Key tasks: Manage the public disclosure of clinical trial information, ensuring timely and accurate posting of trial summaries on international and company websites in accordance with internal rules, external guidelines, and global legislation Provide up to date and consistent Clinical Trial Posting data on required company owned and public websites. Formal quality control of publicly disclosed clinical trial information according to the QA process established.Contribute to the ongoing development and optimization of Bayer’s disclosure processes, adapting to evolving legal,regulatory, and industry requirements Position holder directly interacts with study and product teams, Nuclei, SM teams, RegAff and other CD&O / MA / PV and CH managers and teams. Skills & Qualifications: Education: Bachelor’s degree in Business Administration, Life Sciences, or a related discipline. Understanding of global legislations, regulations and guidelines, i.e. ICH/GCP regulations Understanding of drug development process over different development phases IT Skills at user level and quick learner in IT processes and systems Strong skills in English language, both oral and written (fluent speaking mandatory) Project management: Proven ability to lead and manage cross-functional teams to setup and deliver complex projects in an agile and outcome-focused manner. Exhibit agility and accountability in managing tasks and responsibilities. Be self-organized in prioritizing work, ensuring timely delivery of high-quality results. Solution-oriented mindset, capable of identifying issues and implementing effective solutions in a timely manner. Communication skills: Excellent verbal and written communication skills and ability to explain complex topics in a simplifiedway. Collaboration: Proven ability to collaborate with internal and external stakeholders without hierarchical authority and withaccountability to make decisions. Strong ability to self-organize, pro-actively drive improvement, trouble-shooting, inclusive mindset and strong display of DSO behaviors YOUR APPLICATION This is your opportunity to tackle the world’s biggest challenges with us: Maintaining our health, feeding growing populations and slowing the rate of climate change. You have a voice, ideas and perspectives and we want to hear them. Because our success begins with you. Be part of something big. Be Bayer. Bayer welcomes applications from all individuals, regardless of race, national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, pregnancy, sexual orientation, gender identity, gender expression or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination. Location: Spain : Cataluña : Barcelona Division: Enabling Functions Reference Code: 866480

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Responsibilities

Manage the public disclosure of clinical trial information and result summaries in compliance with global legislation and internal quality standards. Collaborate with cross-functional teams to optimize disclosure processes and ensure data consistency across company and public websites.