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Tas Rights Management Jobs (NOW HIRING)

Advise management and program personnel of contractual rights and obligations * Collaborates with ... Negotiate, review, and prepare NDAs, TAs, Prime Contracts, Subcontracts (e.g. Client, BPA, IDIQ ...

... TAs), Memorandums of Understanding (MOUs), Consultant Agreements, and other business agreements ... Advise management and program teams regarding contractual rights, obligations, risks, and ...

Contracts Administrator

Colorado Springs, CO ยท On-site

$95K - $135K/yr

Advise management and program personnel of contractual rights and obligations * Collaborates with ... Negotiate, review, and prepare NDAs, TAs, Prime Contracts, Subcontracts (e.g. Client, BPA, IDIQ ...

Contracts Administrator

Colorado Springs, CO ยท On-site

$95K - $135K/yr

Advise management and program personnel of contractual rights and obligations * Collaborates with ... Negotiate, review, and prepare NDAs, TAs, Prime Contracts, Subcontracts (e.g. Client, BPA, IDIQ ...

Contracts Administrator

Colorado Springs, CO ยท On-site

$95K - $135K/yr

Advise management and program personnel of contractual rights and obligations * Collaborates with ... Negotiate, review, and prepare NDAs, TAs, Prime Contracts, Subcontracts (e.g. Client, BPA, IDIQ ...

$17/hr

Strong leadership, management, and interpersonal skills. Preferred Qualifications: * College ... Monitor requests of Instructors and TAs for support and respond promptly and appropriately. * Act ...

Showing results 41-60

Tas Rights Management information

What are the key skills and qualifications needed to thrive in the Tas Rights Management position, and why are they important?

To thrive in Tas Rights Management, you need a solid understanding of intellectual property law, licensing, and copyright principles, typically supported by a relevant degree or industry experience. Familiarity with rights management databases, contract management software, and digital rights tracking tools is essential. Strong negotiation, attention to detail, and excellent communication skills distinguish top performers in this field. These skills ensure accurate management and protection of intellectual property assets, while facilitating effective collaborations and minimizing legal risks.

What does a Tas Rights Management do?

In a Tas Rights Management position, your daily responsibilities usually include reviewing and processing licensing agreements, monitoring usage rights for various content, and ensuring legal compliance with intellectual property regulations. You may also be tasked with tracking royalties, communicating with clients and content creators, and maintaining accurate records in digital systems. Collaboration with legal teams, sales departments, and sometimes external partners is common, so teamwork and organization are essential. This dynamic environment offers the chance to build in-depth knowledge of content management and can provide strong foundations for advancing within media, entertainment, or legal industries.

What is a Tas Rights Management?

A Tas Rights Management job involves overseeing intellectual property rights, licensing, and digital content protection. Professionals in this role ensure that copyrighted material is properly managed, licensed, and monetized across platforms. They may work with artists, publishers, and streaming services to prevent unauthorized use and maximize revenue. Strong knowledge of copyright law, digital rights management, and content distribution is often required.

More about Tas Rights Management jobs

What are the most commonly searched types of Tas Rights Management jobs?

The most popular types of Tas Rights Management jobs are:

What states have the most Tas Rights Management jobs?

States with the most job openings for Tas Rights Management jobs include:

Infographic showing various Tas Rights Management job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Executive Director, Center for Scientific Exchange Excellence

MSD Malaysia

North Wales, PA โ€ข On-site

$256 - $403/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 6 hours ago

Posted today


Job description

Job Description The Executive Director, Center for Scientific Exchange Excellence (ED CSEE), position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs (GMSA), Global Medical and Value Capabilities (V&I GMVC), as well as Outcomes Research. This position is a leadership role within V&I GMVC that reports directly to the Vice President, V&I GMVC Lead. The ED CSEE is an integral member of the V&I GMVC Leadership Team providing insight and advice on strategic direction and is accountable for assisting and driving execution of the vision of V&I GMVC and CSEE. This position oversees the CSEE team, integrating both scientific/ therapeutic and engagement/ leadership skills for optimal scientific exchange. This includes the ongoing development and enhancement of Global scientific exchange capabilities by ensuring that appropriate processes, procedures, guidance documents, and tools are in place to enable consistent high quality compliant practices in alignment with company policies. This position leads several core V&I global initiatives, including, but not limited to: Ensuring CSEE support of high-performing teams that engage in scientific exchange, who are viewed by external stakeholders as preferred scientific peers who support their patient care efforts. Collaborating with the network across the V&I organization, including but not limited to, V&I GMSA Therapeutic Areas (TAs) and the V&I GMVC organization (e.g., V&I Operations, Global Scientific & Value Content (GSVC), Global Medical Information (GMI), Global Expert Management and Strategy (GEMS) Consulting & Medical Education, and V&I GMVC Hubs [Europe, Middle East, Africa, Canada Region (EMEAC); Latin America (LATAM); and Asia Pacific Region (AP)]. Implementing CSEE programs that impact across all regions of the V&I organization. CSEE staff in the V&I GMVC Hubs will have a dotted-line reporting relationship into this role.

The application deadline for this position is stated on this posting.

Primary Responsibilities
  • Leadership Set the strategic direction, priorities, operating model, and performance expectations for the CSEE organization across U.S. and global scientific exchange. Accountable for the performance, effectiveness, resource stewardship, and strategic impact of the CSEE department across U.S. and global regions. Lead through managers to build a high-performing, scalable organization with clear accountability, priorities, decision rights, and talent strategies. Serve as a senior member of the V&I GMVC Leadership Team, contributing to enterprise strategy, resource planning, operational prioritization, and execution of organizational objectives. Provide leadership, coaching, and development for CSEE leaders and teams, including talent management, succession planning, performance management, recruitment, retention, and capability building. Represent CSEE priorities and progress in senior leadership forums, including leadership team meetings, operations reviews, summits, town halls, and strategic governance discussions.
  • U.S. and Global Scientific Exchange Strategy Lead execution of the scientific exchange excellence strategy allocating about 50% of time across the U.S. and 50% of time across global-regional scope, ensuring alignment between enterprise standards, regional requirements, and local market needs. Define the enterprise vision and strategic roadmap for scientific exchange excellence, including field medical capabilities, engagement practices, leadership expectations, and capability evolution. Partner with U.S., global, regional, and country Medical Affairs leaders to translate scientific, medical, and business priorities into scalable field medical capability solutions. Provide strategic guidance to regional and country leadership on the planning, deployment, optimization, and evolution of field medical resources and capabilities. Ensure CSEE initiatives enable field medical teams to be recognized by external stakeholders as trusted scientific peers and partners who advance high-quality scientific exchange.
  • Capability, Standards, Training, and Compliance Lead implementation, governance, and continuous improvement of field medical standards, processes, training curricula, guidance documents, tools, and capability programs. Ensure field medical standards and training programs are globally relevant, regionally adaptable, and aligned with company policies, SOPs, legal, privacy, regulatory, and compliance requirements. Collaborate closely with Legal, Compliance, V&I GMVC Operations, GSVC, GMI, GEMS, USMA, GSM TAs, and other stakeholders to ensure integrated and compliant scientific exchange practices. Establish and oversee quality controls, KPIs, monitoring processes, audits, and remediation activities to ensure effective, compliant, and continuously improving scientific exchange practices.
  • Insights, Technology, and Operational Excellence Set the strategic direction for field medical insights collection, evaluation, and knowledge-sharing processes that inform scientific exchange priorities and business decision-making. Partner with V&I GMVC Ops stakeholders to ensure field medical technology solutions are informed by SMEs and support evolving U.S. and global business needs. Identify process improvement opportunities, operational risks, and scalable approaches that enhance efficiency, consistency, and impact across regions and stakeholder groups. Apply strong business and financial acumen to prioritize work, steward resources, evaluate trade-offs, and support sustainable capability delivery across multiple markets and geographies.
  • External Engagement and Industry Leadership Maintain awareness of evolving field medical, scientific exchange, capability development, compliance, and industry best practices, translating relevant trends into actionable organizational improvements. Serve as a company representative with external organizations, industry forums, and benchmarking groups to advance scientific exchange excellence and strengthen organizational credibility and influence. Develop and sustain strategic relationships with internal and external stakeholders to advance scientific exchange priorities, influence organizational decisions, and drive adoption of best practices globally.
Education
  • PharmD, PhD, or MD plus at least 10 years of relevant experience
Required Experience and Skills
  • PharmD, PhD, or MD plus at least 10 years of relevant experience
  • Extensive people leadership experience, including demonstrated success leading leaders, managers, directors, or multi-team organizations
  • Demonstrated ability to lead complex, concurrent, cross-functional initiatives with both U.S. and global/regional scope and impact
  • Proven ability to set strategy, translate priorities into operational plans, and drive execution across multiple groups, geographies, and stakeholder networks
  • Strong business and financial acumen, including ability to evaluate tradeoffs, manage resources, and make recommendations that have long-term organizational impact
  • High level of familiarity with relevant pharmaceutical industry ethical guidelines, compliance expectations, SOPs, risk assessment, and control frameworks
  • Executive presence, strong interpersonal communication and presentation skills, and demonstrated ability to influence senior leaders internally and externally
  • Demonstrated ability to identify process gaps, build scalable solutions, manage change, and innovate practical approaches
  • Ability to travel up to 50% of the time, including national and international travel
Preferred Experience and Skills
  • Minimum of 10 years of biopharmaceutical industry experience with demonstrated excellence in leading, coaching, or enabling field medical/scientific teams
  • Minimum of five years of direct management experience with scientists, clinicians, or field-based medical professionals
  • Deep understanding of Medical Affairs, demonstrated excellence in field medical/scientific exchange, scientific training, engagement excellence, and compliant field medical operating practices
Required Skills
  • Cross-Functional Leadership, Execution Excellence, Executive Leadership, Field Training, Global Experience, Medical Affairs, Operational Business Planning, Pharmaceutical Compliance, Resource Management, Scientific Exchange, Stakeholder Management, Strategic Influence, Training and Development
US and Puerto Rico Residents Only

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.

As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.

For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one anotherโ€™s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is $255,800.00 - $402,700.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employeeโ€™s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 50% Flexible Work Arrangements: Remote Shift: Not Indicated Valid Driving License: No Hazardous Material(s): n/a Job Posting End Date: 08/26/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date.

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

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