When you take on one of our undergraduate placements, you become part of a team that’s working to make the breakthroughs that change patients’ lives, all over the world. You join a workforce in which everyone – no matter what their job title is – comes together to explore, discover and grow. And you help to foster an inclusive culture in which everyone is valued for the unique contribution they make. Current Vacancies Please note that positions for September 2024 will be open for application from August 2023. Business Operations Business Insights Analytics Health and Value Marketing Medical Affairs Regulatory Research and Development

• Lead a global team of Disease Area Leads, Clinical Operations Asset Leads, Third Party Management Leads, to provide leadership and overall delivery of the clinical portfolio. Accountable for the Early and Late Phase strategy and delivery for the TA.

• Coordinate the Business Development strategic input across GCO and be the single point of contact for Alliance Management when business development opportunities are evaluated, including the GCO accountable person for due diligence.

• Partner with key Oncology stakeholders to shape the vision and resourcing/delivery strategy to support the clinical portfolio from design through regulatory submission/approvals.

• Manage, coach, and oversee team members who are accountable for the delivery of clinical development programs working with the key cross-functional leadership teams and project team.

• Strategic leadership and direction for the global clinical delivery team, ensuring alignment with GSK's R&D objectives and overall company strategy.

• Identify and share best practices and oversee the implementation of these into business processes.

• Control and manage the internal budget for global department staff as well as the external project expenditure budget required to deliver the portfolio.

• Provide strategic leadership, management, and a single point of accountability for all aspects of Oncology Clinical Program Delivery worldwide to ensure delivery of key progression targets and optimum alignment with stakeholders.

• Embed innovative approaches to drive delivery optimisation and to accelerate development timelines across the life cycle of an asset.

• Proactively identify and manage risks associated with clinical program delivery. Develop and implement strategies to mitigate risks and ensure the successful execution of clinical trials.

• Create a culture within the organisation that values sharing best practices, fostering a sense of community, identification and development of key talent, innovation and problem-solving in the face of an increasingly challenging environment.

Senior Medical Governance Officer

The role serves to protect the interests of patients and the public, ensuring that Bayer's promotional and non-promotional activities and materials relating to prescription only medicines are carried out in accordance with all relevant legislation and guidelines. These include (but are not limited to) EU directives, UK Medicines Law, the ABPI Code of Practice, MHRA guidelines for the advertising and promotion of medicines in the UK, Advertising Standards Authority (ASA) and company Standard Operating Procedures (SOPs).

In this role, you will support the implementation and ongoing continual improvement of our compliance programme, ensuring alignment with the seven core elements of an effective compliance framework; including establishing and maintaining written policies and procedures, supporting the code compliance committee, delivering effective training and education, fostering open lines of communication, conducting internal monitoring and auditing (self-inspection), enforcing standards through well-publicized disciplinary guidelines, and responding promptly to detected offenses with appropriate corrective actions.
Additionally, you will support Medical Information activities, ensuring accurate and timely dissemination of medical information in compliance with regulatory standards.

TASKS AND RESPONSIBILITIES
•    Effectively conduct activities related to the ‘Core Elements of an Effective Compliance Program’.
•    Responsible for ensuring the development and maintenance of accurate ABPI Code of Practice related Quality System Documents (QSDs) for the UK.
•    Conduct activities related to the UK Local SOP Responsible Person (LSRP) role, overseeing the update and maintenance of all UK QSDs and to represent the UK Medical Department on the topic of UK QSDs during potential internal and external audits and inspections.
•    Be a key member of internal decision-making groups and committees i.e Donations and Grants Committee, Joint Working Collaborative Working Committee.
•    Create and implement highly effective training and validation on the requirements and application of the ABPI Code of Practice and the Medical Governance departments SOPs.
•    Effectively communicate to all stakeholders when there are changes to legislation and guidance, or code updates and case rulings that could have an impact on Bayer pharma policies, processes.
•    Be responsible for the completion of regular process checks for both Head Office and Field Force activities, including the identification of corrective and preventative actions (CAPAs) and overseeing and their documenting and completion.
•    Collaborate with cross-functional Bayer colleagues to provide expertise and advice regarding the ABPI Code of Practice and related Bayer QSDs.
•    Support and provide cover for local Medical Information related activities for the UK and Ireland, including responding to Medical Information enquiries (when required), examination of local Medical Information responses, and conducting Quality Control checks of Medical Information responses to ensure are carried out in accordance with relevant requirements.
•    Undertake additional activities, as deemed necessary for the role.

Key Working Relation:
•    Effectively collaborate with the Strategic Expert, Medical Governance to review work in progress, prioritize demands, identify issues of operational importance and identify solutions to enable timely execution of business activities.
•    Within the Company: Colleagues from the cross-functional pharmaceutical division, country platform functions and the global LQSD and Medical Information team(s).
•    Outside the Company: Healthcare Professionals and Other Relevant Decision Makers (ORDMs), Prescriptions Medicines Code of Practice Authority (PMCPA), Regulators (MHRA), Compliance Consultants and third-party service providers.

We have an exciting opportunity for a Farm Worker who will report to the Farm Manager at our Field Stations in Little Shelford and Great Chishill. Our field stations provide support to the global Agronomic Development program and EU zonal development programm for our products. Bayer CropScience owns two Field Stations, which require particular agronomic practices in order to facilitate effective Field Trials and residue work to GEP or GLP standards. The field station team also provides drilling and harvesting support to regionally based agronomists.

The primary responsibilities of this role are to:

• Develop code in multiple programming languages (e.g., Python, R, etc.);

• Support mining of process data from IT systems and databases;

• Develop workflows for mining, pre-processing and visualization of data;

• Evaluate and apply different machine learning and advanced statistical methods;

• Communicate outcome of development activities to the team;

• Document project outcome in a short technical report.

Scientific Expertise

• Complete core training curriculum and basic MSL and Therapeutic Area (TA) Certification;

• Demonstrated accountability to continuous learning and growth (Franchise data, MSL role, Soft Skills, Personal Development).  Completes recertification where applicable;

• Professional licensure with CEU documentation where applicable;

• Depth of knowledge within the therapeutic area exceeds that of peers and/or Medical Affairs experience in multiple therapeutic areas;

• Coordinates and lead TA updates, team discussions, training initiatives (i.e. journal clubs);

• Attend and report on local, regional and national medical conferences and other meetings of value;

• Coordinate team coverage of major regional or national meetings including program evaluation, required attendance and coordination of high quality meeting reports;

• Identifies educational gaps and provides subsequent recommendations for educational resource, content, or initiative development.

External HCP and Stakeholder Engagement

• Establishes robust long-term relationships with Thought Leaders and other key stakeholders through education on up to date scientific information in alignment with US, Global, and Area Business Unit definitions and strategies;

• Impactful proactive engagement with TLs, HCPs, research sites, associations, societies, & other stakeholders according to defined scope and engagement plans.  Actively seeks future stakeholders and emerging Thought Leader groups in alignment with local health care system and medical strategy;

• Leverage knowledge of US and Global definitions and strategies to develop and pull through local Area Business Unit strategy;

• Responsible and Accountable for driving medical strategy by translating the local medical plan into implementable TL and stakeholder engagement strategies with cross-functional teams and identify synergies with the interests of Bayer and the general medical community;

• Approach accounts, customers, and Area Business Unit strategically, utilizing key metrics to ensure alignment to territory plan and medical objectives;

• Compliantly supports speaker training and evaluation and medical evaluation of scientific merit;

• Advisory Board or other Bayer Program coordination or support during meeting;

• Coordinates TL engagement with Franchise Medical Affairs team and relevant internal stakeholders.

Education

• Delivers educational presentations to external audiences, stakeholders, and customers groups.  Proactive identification of educational opportunities within assigned Area Business Unit to stakeholders or customers groups;

• Responsible for timely, accurate, specific and balanced responses to Medical Inquires in collaboration with Medical Communications;

• Adherence to SOP and FDA guidance for distribution of scientific information;

• Adherence to SOP and compliance guidelines for all external contacts;

• Prepares and presents data to internal audiences including MA and Commercial partners.

Research

• Responsible for supporting research projects aligned with medical and brand strategy; including facilitating investigator-initiated research (IIR) and research site identification;

• Responsible for supporting clinical trial team and engaging with appropriate stakeholders for Bayer sponsored clinical trials. Support with data collection, feasibility & initiation visits, and study support as appropriate.

Insights

• Responsible and Accountable for generating relevant HCP and stakeholder insights that deepen understanding of patients, HCPs, consumers, or treatment landscape.  Document and communicate them accordingly within system or to stakeholders to inform, refine, and enhance tactics and strategy;

• Report new compound development information and potential collaborations when appropriate or requested in line with corporate strategy.

Collaboration

• Compliant active strategic partnership and collaboration with territory cross-functional stakeholders (i.e. Area General Manager, Area Business Unit team, Field DGOS, etc.) as part of Area Business Unit team;

• Presentations to internal audiences including Therapeutic Area Medical Affairs (MA) or commercial partners;

• Lead project teams or task forces as appropriate within Franchise Medical Team;

• Initiates best practice discussions for MSL team and internal partners;

• Responsible and accountable as MSL mentor as appropriate.

New Ways of Working (Data Collection / Analysis / Interpretation)

• Internal champion of new ways of working including platforms, systems, capabilities.  Train, mentor, and empower Field Medical team to leverage new ways of working;

• Complete all required customer activity documentation, training, expense reporting, and other administrative responsibilities in a timely, accurate, and compliant manner;

• Responsible for reviewing and interpreting interaction analytics related to TL engagement and take appropriate actions to execute stakeholder plans;

• Use data and analytics to seek out and maximize customer engagement opportunities within the territory;

• Leverage evolving country and Global platforms and systems to ensure data driven tailored approach to customer engagement;

• Leverage omnichannel methods of engagement with stakeholders to ensure customer-centric approach to data dissemination and education.

ROLE SUMMARY

• Develops model informed drug development (MIDD) plans across projects and disease areas in order to optimize prospective studies, inform drug development strategy and project decision-making, in collaboration with partners.

• Conducts and reports quantitative analyses which integrate knowledge of pharmacokinetics, pharmacodynamics, patient characteristics, and disease states to optimize doses, dosage regimens and study designs throughout clinical drug development.

• Identifies opportunities where modeling and simulation can advance the understanding of pharmacological activity, efficacy and safety.

• Support and/or develop pharmacometrics tools, automation workflows, software, and related business processes

ROLE RESPONSIBILITIES

• Provide support in the development of quantitative methodology, pharmacometrics tools, software, hardware, and/or related business processes.

• With guidance, provide MIDD expertise on multidisciplinary development teams, working closely with clinical pharmacologists, clinicians, and statisticians to create MIDD plans that include assessments of a drug’s efficacy, safety, and commercial viability.

• Responsible for the planning and execution of relevant quantitative analyses which may include population pharmacokinetics, pharmacokinetics/pharmacodynamics, exposure response, disease progression modeling, model-based meta analysis, and decision analysis for multiple analyses supporting a program.

• Prepare formal presentations and written reports to Pfizer standards.

• Contribute to regulatory documents (summary documents, briefing books, regulatory responses)

• Have a good understanding of literature, government guidelines, and internal guidance as relates to pharmacometrics and MIDD

• Contribute to the development or improvement of our tools, processes and methodology, including involvement in internal cross-functional workgroups or initiatives, external alliances or committees, consortia and academic relationships

PURPOSE

To position Bayer for success and growth, we are investing in our Digital Analytics capabilities within our US Pharmaceutical Data Science and Customer Insights team. As part of the team, you will help us expand an industry-leading in-house digital marketing analytics function, supporting key growth product(s) in Bayer’s US Pharmaceutical portfolio. You will use your expertise in digital media and advanced analytics to translate data into insights and actions that will maximize our strategic investments in media & data infrastructure. At Bayer, our culture is collegial and highly collaborative, and success hinges on proactive ownership of responsibilities, innovative thinking, and the ability to work collaboratively with teams across Insights & Analytics, Digital Strategy & Product Operations, and Brand Marketing.

YOUR TASKS AND RESPONSIBILITIES

• Provide cross-functional teams with actionable insights to optimize the effectiveness and efficiency of digital marketing tactics and campaigns within core digital channels: website, email, search, banner/display, social, video/TV, and out of home/point of care;

• Collaborate with our in-house digital media, digital strategy, digital ops, and data solutions teams to oversee measurement operations, guiding tagging/tracking strategy & process, measurement planning, and KPI setting to deliver on an industry-leading digital analytics approach;

• Leverage analytical techniques within and across marketing channels to deliver rapid, actionable, and comprehensive insights designed to establish cross-channel best practices, inform marketing/media optimization, and guide customer and channel strategy;

• Oversee the design, execution, and analysis of pilots and A/B and multivariate tests for media, targeting, and content/messaging to ensure that tests yield interpretable and actionable results;

• Proactively identify opportunities for analyses that identify and establish data-driven best practices; evangelize results across brand marketing and strategic stakeholders to ensure adoption of those best practices;

• Translate analytics into actionable insights and recommendations; communicate insights and recommendations clearly to both leadership and tactical/executional teams;

• Collaborate with and direct external media and analytics partners to coordinate supplemental analytics studies and broader analytics/data integrations;

• Collaborate closely with Digital Media, Digital Strategy, Advanced Analytics, Insights & Analytics, and Commercial Data Solutions teams to understand strategy and tactics and ensure communication and activation of analytics-driven insights across teams;

• Integrate seamlessly with other team members within Insights & Analytics to add a digital perspective to business insights reporting; opportunity to support analytics efforts outside of digital (e.g. business analytics, market research, market access).

• The primary location for this role is Whippany, NJ.  Candidates must be easily commutable to the Whippany, NJ site at least 2-3 days per week.  Candidates not easily commutable to the area must be willing/able to relocate as a remote arrangement is not available for this role.

• Visa sponsorship may be available for this role.