Urwah Admin

Boehringer Ingelheim

<div></div><div><div><div><div><p>The Vice President, Experimental Medicine &ndash; Inflammation Gastroenterology and Rheumatology will provide strategic and visionary leadership for early clinical development and global experimental medicine within Gastroenterology and Rheumatology. This VP role is critical to accelerating proof-of-concept studies, shaping global strategy, and ensuring competitive differentiation. This role will drive innovation and scientific excellence to integrate translational science, influence portfolio decisions, and deliver transformative therapies aligned with corporate objectives.
</p><p>This role has enterprise-wide impact through portfolio acceleration, external scientific leadership, and cross-functional integration with regulatory, clinical operations, and commercial strategies globally.
</p><p>As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunities for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
</p></div></div><div><div><h2 class="jobSectionHeader"><b>Duties &amp; Responsibilities
</b></h2></div><div><p>Strategic Leadership:
</p><ul><li>Defines and executes global medical and scientific strategy for the TA.
</li><li>Serves as a key decision-maker in governance committees.
</li>Responsible for timely delivery of early-phase clinical plans; alignment with portfolio strategy.<br>
<li>
</li></ul><p><br>
Scientific &amp; Clinical Excellence:
</p><ul><li>Oversees design and conduct of Phase I&ndash;IIb, ensuring scientific rigor and regulatory compliance.
</li><li>Maintains deep knowledge of emerging science and competitor strategies.
</li><li>Oversees alignment of scientific platforms, medical communication, and product optimization plans.
</li>Reviews and approves protocols, reports, and publications.<br>
<li>
</li></ul><p><br>
Team Leadership:
</p><ul><li>Builds and inspires high-performing global teams, including clinical scientists and physicians.
</li>Fosters innovation and operational excellence.<br>
<li>
</li></ul><p><br>
Cross-Functional Collaboration:
</p><ul><li>Partners with Research, Safety Science, Clinical Pharmacology, Translational Medicine, Regulatory, and Commercial teams.
</li>Responsible for effective governance participation; stakeholder satisfaction.<br>
<li>
</li></ul><p><br>
Business Development &amp; External Engagement:
</p><ul><li>Leads preliminary clinical evaluations for in-licensing opportunities.
</li><li>Represents the organization externally with key opinion leaders and regulatory authorities.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Requirements
</b></h2></div><div><ul><li>MD or MD/PhD in relevant medical specialty/Therapeutic Area required.
</li><li>Scientific Expertise: Deep understanding of disease biology, clinical trial design, and translational medicine.
</li><li>Leadership: Ability to inspire and lead multidisciplinary teams.
</li><li>Strategic Thinking: Strong capability to define and execute long-term vision.
</li><li>Communication: Excellent ability to influence and engage internal and external stakeholders.
</li><li>Regulatory Knowledge: Familiarity with global drug development and compliance requirements.
</li>Innovation: Track record of implementing novel approaches in early clinical development.<br>
<li>
</li></ul><p><br>
<b>Eligibility Requirements </b>:
</p><ul><li>Must be legally authorized to work in the United States without restriction.
</li><li>Must be willing to take a drug test and post-offer physical (if required).
</li><li>Must be 18 years of age or older.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Desired Skills, Experience and Abilities</b></h2></div></div></div></div><div></div>

Vice President, Experimental Medicine - Inflammation

<div></div><div><div><div><div><p>As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.<br>
</p><p></p><p>The Senior Associate Director (SAD) Site Management Lead will support the Executive Director Site Management &amp; Monitoring to oversee US clinical programs effectively and efficiently across multiple therapeutic areas in full compliance with GCP/ICH, quality, safety of patients and business goals. The SR AD, Site Management Lead is responsible for forecasting and providing oversight of resources supporting US Clinical Trial Managers (CTMs)and managing the Site Enablement and IC teams. This role is responsible for resources and direct reports under the oversight of the SAD Site Management Lead are responsible for the Site Management and Regulatory Ethics Committee/Institutional Review Board (IRB) submissions, inclusive of trial participation and informed consent to ensure activities on clinical trials are completed in accordance to milestones, timelines and quality.<br>
</p><p></p><p>The SR AD, Site Management Lead is accountable for end-to-end site management including resource forecasting, on-boarding, and performance tracking for FSP/ISP staff across all US clinical programs across Therapeutic areas, i.e., Clinical Associates (CAs), Clinical Trial Operations Specialist (CTOS), Regulatory Start Up Specialist (RSUS), Informed Consent Specialist (ICS) Site Activation Manager (SAM), Establishes standards. This role collaborates with internal stakeholders to support the allocation of resources and coordination of all staffing decisions. The incumbent is responsible for providing direction and management for direct reports assigned Site Management activities supporting trials conducted within Therapeutic Area(s). The CD&amp;O line manager is responsible for providing strong leadership that is aligned to the HPBU intent, Medicine and CD&amp;O vision, strategies, goals, and operating model to ensure successful delivery (speed &amp; value) of clinical trials in the team.<br>
</p><p></p><p>The line manager is responsible for the execution, delivery and oversight of high-quality clinical trials that meet pipeline commitments, specific scientific medical, and regulatory requirements in the team as well as responsible for team performance oversight and excellence. This role embraces innovative technologies, as well as creates and maintains a culture that drives empowerment, smart risk talking and one common CD&amp;O identity.
</p></div></div><div><div><h2 class="jobSectionHeader"><b>Duties &amp; Responsibilities
</b></h2></div><div><ul><li>Builds, develops and maintains close working relationships with Clinical Development &amp; Operations (CD&amp;O) functional groups, e.g., Legal, Ethics &amp; Compliance and third-party vendors including CROs, IRBs to assure a closely coordinated program of activities based on common objectives and focusing on value, quality and operational efficiencies.
</li><li>Provides leadership and strategic direction to the Site Enablement Team.
</li><li>Maintains oversight of the trials at all stages of conduct to ensure operational vendor oversight;
</li><li>Ensures delivery of site management activities and regulatory document collection (review, and approval of site essential documents, including placement in relevant systems (e.g., Clinergize)) is executed per regulations, process and in accordance with business needs.
</li><li>Provides comprehensive oversight of all regulatory submissions to IRB across all trials and therapeutic areas.
</li><li>Identifies and communicates operational issues and trends across the portfolio of trials based on input from 3rd party vendor(s), Regulatory Start Up Specialists (RSUS), trial team, and/or IRB vendor.
</li><li>Implements corrective actions/process improvements inclusive of audit findings and CAPAs to maintain and enhance overall trial execution and quality; represents all site management and regulatory document activities across trial portfolio. Oversee external Site Management FSP/ISP resources ~ 100-150.
</li><li>Leads continuous improvement strategies within the Site Management group and identifies ways to streamline work processes to support quality improvement initiatives.
</li><li>Leads and/or represents Site Management function as Subject Matter Expert (SME) on local/global working groups.
</li><li>Leads Site Management inspection readiness activities, participates in Sponsor Inspections and support research site health authority inspection(s).
</li><li>Ensures quality and compliance in support of regulatory applications;
</li><li>Supports leadership in qualifying vendors (e.g., IRB).
</li><li>Oversees and maintains accountability for Key Performance Indicators (KPIs) as provided by internal and external stakeholders vendor(s).
</li><li>Liaises and escalates as appropriate with BIPI Vendor Management to maintain quality and enhance performance of the operating model.
</li><li>Projects and forecasts current/future resourcing needs to ensure business continuity; ensures appropriate allocation and capacity planning to optimize utilization of resources.
</li><li>Identifies trends and implements effective change to maximize efficiencies and utilization of resource(s).
</li><li>Manages functional budgets, including resource projections, capacity assessments and vendor(s)(e.g. FSP, ISP)oversight and evaluation of services in the Site Management Function, to ensure adequate and appropriate resourcing for the on-time delivery of all trials in the BIPI portfolio.
</li><li>Guides efforts of third-party vendor(s) to ensure deliverables assigned to resources are completed to high quality within planned timelines.
</li><li>Monitors and approves service invoices, as appropriate.
</li><li>Maintains a focused continuous improvement culture by identifying and executing strategies and priorities to enable milestone delivery and to enhance overall operational effectiveness.
</li><li>Actively remains current with industry standards, trends, and competitive intelligence and best practices.
</li><li>Identifies, develops and implements process improvements (e.g., SOP/KM Assets/HTGs) to drive efficiencies, ensure consistency and alignment across CD&amp;O.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Requirements
</b></h2></div><div><ul><li>Bachelor degree (preferred major/focus: Health Sciences, Health Care, Nursing or Others) with 7 years relevant experience.
</li><li>OR
</li><li>Masters or Advanced degree with five-plus (5+) years&rsquo; experience.
</li><li>Minimum three (3) year of direct/matrix line management experience.
</li><li>Demonstrated experience in the regulated pharmaceutical or healthcare industry with a focus on operational and technical experience managing regulatory document work packages across the life cycle of a clinical trial.
</li><li>Advanced understanding of all phases of drug development (I-IV) as well as knowledge to implement FDA/ICH/GCP/HIPAA regulations, guidance, and legal understanding.
</li><li>Understanding of Federal Regulations pertaining to IND and NDA regulations.
</li><li>Track record in setting priorities, organization and problem-solving skills which support and enable sound decision making.
</li><li>Excellent customer service skills and high attention to detail.
</li><li>Demonstrated analytical skills and critical thinking with the ability to proactively identify and resolve issues with a solutions-oriented approach in a variety of complex situations requiring new solutions.
</li><li>Experience initiating and leading department and cross-functional strategic initiatives.
</li><li>Proficient written and verbal communication skills and the ability to be clear and concise in a variety of communication settings.
</li><li>Proficient organizational and effective time management skills with the ability to work well under pressure.
</li><li>Exercise sound judgment in planning and accomplishing goals.
</li><li>Ability to use and learn system applications, e.g., MS Office, document management systems, etc.
</li>Ability to travel overnight domestically and/or internationally, as needed.<br>
<li>
</li></ul><p><br>
<b>Eligibility Requirements </b>:
</p><ul><li>Must be legally authorized to work in the United States without restriction.
</li><li>Must be willing to take a drug test and post-offer physical (if required).
</li><li>Must be 18 years of age or older.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Compensation</b></h2></div></div></div></div><p></p>

SR Assoc Director, Site Management Lead (Hybrid/On-site)

<div><p><b>THE POSITION
</b></p><p>We are looking for a Medical Sales Representative based in Egypt. This position will be responsible in effectively representing and promoting Boehringer Ingelheim (BI) core products to existing and potential customers, by presenting the benefits of BI products, with the objective of maximizing sales revenue and increasing market share. Key responsibilities in this role include offering innovative, tailored solutions to ensure long term presence of the CRM portfolio whilst adhering to company best practices. This position will be reporting to the district manager.<br>
</p><p></p><p><b>Tasks &amp; Responsibilities:
</b></p><ul><li>Sales Planning:
</li></ul><p>Builds and executes an effective Sales Action Plan with the objective of maximizing business in assigned territories and to ensure achievement of sales and market share targets/objectives Monitors the sales development and performance of Boehringer Ingelheim CRM products
</p><ul><li>Sales Execution:
</li></ul><p>Works closely with district Sales Manager in executing an effective Sales Action Plan with the objective of maximizing business in assigned districts to ensure achievement of district sales targets/objectives
</p><p>Plan and schedule daily visits with existing and potential customers to deliver the company's core product messages
</p><p>Record and monitor product sales and obtain feedback from existing customers on product performance and activity
</p><p>Secure a consistent and sustainable growth in sales and revenue by identifying and developing new market opportunities
</p><ul><li>Stakeholder Management:
</li></ul><p>Build strong and long partnerships with all key stakeholders and ensure their full awareness of Boehringer Ingelheim product benefit.
</p><p>Propose customized partnership programs for existing and future customers that need to build productive relations between them and the company<br>
</p><p></p><p><b>Requirements:
</b></p><p>Bachelor&rsquo;s degree
</p><p>Minimum of 2 years' experience in the Market
</p><p>Previous experience in Cardio, Renal, Metabolic therapeutic areas is a plus Excellent communication and presentation skills
</p><p>Ability to build and maintain relations with internal and external stakeholders.<br>
</p><p></p><p><b>What&rsquo;s Next?
</b></p><p>We are looking forward to receiving your application! We will then have a look at your profile. If we see a match, we will invite you for a screening interview.
</p><p><b>Screening:
</b></p><p>In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (&ldquo;SPL&rdquo;). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.</p></div>

Medical Representative - CRM

<div><p><b>The Opportunity
</b></p><p>We are looking for a <b>Medical Representative </b>based in Riyadh. This position will be reporting to the Regional Sales Manager.<br>
</p><p></p><p><b>Purpose </b>:
</p><p>Promote of BI products to Health Care professionals ensuring their appropriate use and adherence to local regulatory and pharma code requirements by
 </p><ul><li>Defining &amp; executing sales account plans, based on the local activity/expert engagement plan
 </li></ul><ul><li>Being accountable for maximizing the number of appropriate patients that receive Boehringer Ingelheims products by creating added value to the key stakeholders<br>
</li></ul><p></p><p><b>Responsibility </b>:
</p><p>Promote BI products, with adherence to local regulatory and pharma code requirements. If applicable, handle and distribute product samples in accordance to current Good Distribution Practices, applicable laws and regulations.
</p><p>Achieve sales &amp; market share objectives by maximizing the number of appropriate patients that receive Boehringer Ingelheim products
</p><p>Define and execute flawless aligned sales account plans, based on the local activity/expert engagement plan, e.g.
</p><ul><li>Analysing and profiling customers
</li></ul><ul><li>Developing, creating, managing, executing and following up integrated customer plans
</li></ul><ul><li>Implementing customer engagement model, according to the adoption ladder and brand strategy
</li></ul><p>Orchestrate a customer centric engagement through collaboration by cross-functional and external stakeholders, e.g.
</p><ul><li>Integrated Customer Engagement
</li></ul><ul><li>Managing all customers/stakeholders interactions: Face-to-face, Digital, Congresses and CME
</li></ul><ul><li>Using DDA&rsquo;s and/or other approved and scientifical materials as basis for Health Care Professional&rsquo;s discussions
</li></ul><ul><li>Feeding back market info (e.g. competitive intelligence, own products, campaign, messaging to Brand Teams)<br>
</li></ul><p></p><p><b>Educational background:
</b></p><p>Bachelor in pharma<br>
</p><p></p><p><b>Required skills:
</b></p><ul><li>Entrepreneurship
</li><li>Effective Communication
</li><li>Analytical skills and planning
</li><li>Influencing skills
</li><li>Agility
</li><li>Accountability
</li><li>Negotiation
</li>Business Acumen<br>
<li>
</li></ul><p></p><p><b>What&rsquo;s Next?
</b></p><p>We are looking forward to receiving your application! We will then have a look at your profile. If we see a match, we will invite you for a screening interview.<br>
</p><p></p><p><b>Screening:
</b></p><p>In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (&ldquo;SPL&rdquo;). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection</p></div>

Medical Representative

<div><p><b>We are hiring a Medical Representative in Abu Dhabi, UAE.
</b></p><p>The successful candidate will be responsible for effectively representing and promoting Boehringer Ingelheim (BI) core products to existing and potential customers. S/he consults with and provides clinical and technical information to healthcare professionals within the assigned territory and in compliance with Boehringer Ingelheim&rsquo;s standard operational procedures and the Ministry of Health practices.
 </p><p>The job holder will be based in Abu Dhabi/UAE and will report directly to the District Manager.
<br>
<br>
<b>Responsibilities
</b></p><ul><li>Execute an effective Sales Action Plan with the objective to build and sustain long-term customer partnerships with key accounts that create mutual value.
</li><li>Achieve business plans, enlisting brand objectives and the annual target.
</li><li>Perform and report on competitive intelligence activities on key accounts.
</li><li>Coordinate and participate along with the Marketing Department in prelaunch and launch activities, Audio Visual and CME meetings, etc.
</li><li>Develop and maintain relations with HCPs.
</li><li>Prepare periodical activity tracker and sales-related reports/objectives.
</li></ul><p><b>Requirements:
</b></p><ul><li>Bachelor&rsquo;s degree in pharmacy, Medicine or any other relevant field
</li><li>2-3 years similar work experience preferably in a multinational pharmaceutical company
</li><li>A minimum of 1 year experience within cardio-metabolic therapy area is preferred.
</li><li>Minimum 1 year experience in a similar role in UAE is required.
</li><li>Possesses a valid UAE driver&rsquo;s license.
</li><li>Fluent in English&amp;Arabic
</li><li>Proficient in Microsoft Office Applications
</li></ul><p><b>Competencies:
</b></p><ul><li>Customer-centric
</li><li>Detail and results orientated.
</li><li>Innovative and Problem solver
</li><li>Good presentation and negotiation skills
</li><li>Can work under pressure.
</li><li>Team player
</li><li>Good personal leadership
</li><li>Good administration skills</li></ul></div>

<div></div><div><div><div><div><p>As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunities for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
<br>
<br>
The Materials and Inventory Control Manager is responsible for leading the Purchase Team of direct materials and managing the Inventory Control of Finish Goods, Intermediates, Raw Materials and Packaging Components. This role will be responsible for developing and maintaining inventory targets for internal goals and VMI levels. The incumbent will be responsible for management of performing accurate and timely analysis of the Material Resource Planning MRP) in SAP to manage supply of material including planning and procuring of materials based on master production schedules and creating monthly purchasing planning schedules for Warehouse and Quality areas considering their capacities.
<br>
<br>
The Materials and Inventory Control Manager is responsible for analyzing existing production materials inventories to identify and prevent IQV items, slow movers, revaluations, expiration and obsolete materials. This role is responsible for issuing materials forecast, purchase orders, tracking orders, resolving discrepancies in orders or accounts, monitoring the performance of suppliers and issuing OTIF reports. The incumbent is responsible to update monthly production schedules based on material status, maintain accurate master data in SAP system, establish depletion plan for art changes and meet current inventory policy. This position serves as liaison between groups such as Suppliers, Quality and Sourcing areas. for the integrity of inventory for finished goods, raw materials, intermediate and components, and supporting systems for the applicable warehouses including 3rd party inventory.
<br>
<br>
The Materials and Inventory Control Manager will support domestic and international finished goods order management and distribution including outbound deliveries. This role is responsible for creating, tracking and reporting relevant analytics and KPIs. The incumbent will determine and enforce site best practice for processing routine and non-routine material transactions within the ERP system.
</p></div></div><div><div><h2 class="jobSectionHeader"><b>Duties &amp; Responsibilities
</b></h2></div><div><ul><li>Responsible for maintaining high standards for personnel performance, training and development in accordance with the personnel policies of the company, establishing a high level of morale, and teamwork throughout the department.
</li><li>Makes use of work teams, and weekly communication meetings.
</li><li>Implements departmental policies &amp; procedures in accordance with company policies, procedures, goals and objectives.
</li><li>The Manager is highly technical with ERP Inventory Management Systems and leads activities related to the integrity of inventory accuracy throughout supply chain by establishing best practices with SAP inventory transaction processes to support financial and business strategies and objectives. This includes the balancing of the Warehouse for local and 3rd party Inventory Management in SAP, reconciliations, and root cause analysis of reconciliations.
</li><li>Leads large departmental or cross functional projects pertaining to material flow and supporting SAP system support and improvements. Site Lead for relevant SAP updates, site training for cross stream functions and transactional system support.
</li><li>Leads day-to-day technical support to Physical Distribution Operations and Site Warehousing Operations, and Production Operations.
</li><li>Identifies &amp; leads implementation of potential technology and process improvement opportunities to improve Agility and efficiency in anticipation of evolving business requirements.
</li><li>Leads department in the completion of departmental initiatives that align and support the company's overall strategy.
</li><li>Responsible for periodic and ad hoc business analyses and KPI's as requested.
</li><li>Provides documentation and responses for auditor requests in an accurate and timely manner to the audit lead. No audit findings pertaining to Inventory Control.
</li>Acts as a back-up to direct reports to assure consistent operations of routine and critical functions.<br>
<li>
</li></ul><p><br>
Leads direct materials purchasing activities that include:
</p><ul><li>Analyzing MRP SAP system to ensure accuracy and updates information and entries on a weekly basis.
</li><li>Creating purchase requisitions in SAP system.
</li><li>Preparing production material forecast reports to ensure that purchasing contracts can be updated.
</li><li>Negotiating credits with supplier and/or markets.
</li><li>Creating schedules for Warehouse and Quality areas.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Requirements
</b></h2></div><div><ul><li>Bachelor's Degree in related Business, Operations, Supply Chain, or related field from an accredited institution.
</li><li>Minimum of five (5) years of experience in purchasing and inventory management with a minimum of four (4) years of management experience.
</li><li>APICS certification is preferred.
</li><li>Demonstrated ability to train and develop others.
</li><li>Demonstrates the ability to lead and follow systematic continuous improvement methodologies and the willingness to identify, define, and implement process improvements.
</li><li>Proficient with word processing, spreadsheets, and database management required.
</li><li>Must be detail oriented, able to work with minimal supervision and self-motivated to utilize resources to troubleshoot as needed.
</li><li>Ability to manage multiple on-going projects with aggressive deadlines.
</li><li>Strong proofreading skills along with excellent communication and written capabilities.
</li><li>Must be proficient in MS office applications such as Word, Excel, Outlook, etc.
</li>Must be able to readily learn and quickly become proficient in all software applications utilized for packaging equipment and operations.<br>
<li>
</li></ul><p><br>
<b>Eligibility Requirements </b>:
</p><ul><li>Must be legally authorized to work in the United States without restriction.
</li><li>Must be willing to take a drug test and post-offer physical (if required).
</li><li>Must be 18 years of age or older.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Desired Skills, Experience and Abilities</b></h2></div></div></div></div><div></div>

Materials and Inventory Control Manager

<div></div><div><div><div><div><p>As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
<br>
<br>
The Executive Director, Animal Health Business Law is the senior legal advisor for BIAH USA Commercial Business, leading a high-performing legal and brand security team. This role will provide strategic legal counsel, drive operational excellence, and enable compliant innovation across a $2.4+B business. The incumbent provides a broad range of legal services, to clients at the CMC level or below as member of the Commercial Leadership Team. The level of counseling provided requires in depth knowledge of the business, management, and legal and regulatory environment; and the ability to communicate the legal risks associated with making specific strategic decisions. The impact of all legal advice provided at this level is extremely high, as President of BIAH USA and strategic decision makers incorporate expert counsel into their decision-making process.
</p></div></div><div><div><h2 class="jobSectionHeader"><b>Duties &amp; Responsibilities
</b></h2></div><div><ul><li>Is the Primary Legal Advisor to President, BIAH USA and US AH Commercial Leadership Team.
</li><li>Due to pervasive level of regulation, position requires knowledge and provision of advice on wide range of legal topics (e.g., FDA/EPA/USDA/FTC regulations and antitrust regulations).
</li><li>Is a Member of BIAH USA Commercial Leadership Team and BIAH USA Legal Leadership Team.
</li><li>Is a Strategic Business Partner to senior business leaders.
</li><li>Drives cross-functional collaboration to deliver operational excellence in legal services.
</li><li>Accountable for, in close coordination with Compliance Officer and VP, Litigation, compliance &amp; risk management within US AH commercial teams and activities, as well commercial litigation &amp; dispute resolution.
</li><li>Manages a team of five (5), including three (3) attorneys, one (1) paralegal and one (1) brand security expert.
</li><li>Mentors and trains attorneys, paralegals and other personnel within department.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Requirements
</b></h2></div><div><ul><li>Juris Doctorate required.
</li><li>Six-plus (6+) year&rsquo;s leadership experience (i.e., leading employees, leading leaders, leading projects, leading business/functions).
</li><li>Substantive legal knowledge and experience in areas of operations and regulatory law.
</li><li>Knowledge of animal health or pharmaceutical industry; substantive understanding of compliance-related issues; general knowledge of litigation and risk management.
</li><li>Understanding of regulatory and political changes on state, national, and international levels.
</li><li>Strong business acumen, legal expertise, and negotiation skills.
</li><li>Ability to evaluate risk and willingness to assume prudent risks.
</li>High emotional intelligence and people leadership.<br>
<li>
</li></ul><p><br>
<b>Eligibility Requirements </b>:
</p><ul><li>Must be legally authorized to work in the United States without restriction.
</li><li>Must be willing to take a drug test and post-offer physical (if required).
</li><li>Must be 18 years of age or older.</li></ul></div></div></div></div>

Executive Director, Animal Health Business Law

Join Boehringer Ingelheim and explore 22   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Boehringer Ingelheim

ABOUT_COMPANY

Vice President, Experimental Medicine - Inflammation

SR Assoc Director, Site Management Lead (Hybrid/On-site)

Medical Representative - CRM

Medical Representative

Medical Representative

Materials and Inventory Control Manager

Executive Director, Animal Health Business Law