3 publicaciones de empleo destacadas de sr site contract specialist en buenos aires, b (¡Están contratando!)

Sr Site Contract Specialist
Thermo Fisher Scientific —Buenos Aires, Buenos Aires
- Tiempo completo
Sr. Site Contracts Associate, IQVIA Biotech
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
Sr. Safety Specialist
サイネオス・ヘルス —Buenos Aires, Buenos Aires
5d

More jobs to discover

Find similar jobs that you might be interested in.

Sr. Site Contracts Associate, IQVIA Biotech
IQVIA —Buenos Aires, Buenos Aires
3-5-year relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable global and/or regional experience…
Site Contracts Associate, IQVIA Biotech
IQVIA —Buenos Aires, Buenos Aires
Experience in clinical trial budgeting, contracting, or site management strongly preferred. This role plays a critical part in ensuring timely and compliant…
9d

Quiero recibir la alerta de empleo más reciente para sr site contract specialist en buenos aires, b

Al ingresar a tu cuenta, aceptas las Condiciones del servicio de SimplyHired y das tu consentimiento a nuestra Política de privacidad y Cookies.

Explorar empleos en más ubicaciones

sr site contract specialist jobs near buenos aires, b

Empleos de Intelligence Specialist en Buenos Aires, Buenos Aires

Empleos de Language Specialist en Desde Casa

Empleos de Analista Contable Senior en Capital Federal, Buenos Aires

Empleos de Operations Specialist Ecommerce en Provincia De Buenos Aires

Empleos de E Commerce Specialist en Buenos Aires, Buenos Aires

Empleos de Analista Funcional Senior en Capital Federal, Buenos Aires

Sr Site Contract Specialist

Thermo Fisher Scientific -
Buenos Aires, Buenos Aires

Postulate ahora

Detalles del empleo

Tiempo completo

Descripción completa del empleo

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Sr Site Contract Specialist

Make an Impact at the Forefront of Innovation

At Thermo Fisher Scientific, our Clinical Research team supports leading pharmaceutical, biotechnology, and emerging biopharma companies in advancing innovative therapies worldwide. Having contributed to thousands of clinical trials across more than 100 countries, we are committed to accelerating research that improves patient lives.

As a Senior Site Contract Specialist, you will play a critical role in the successful start-up and execution of clinical trials by leading site contract and budget negotiations. Working closely with investigative sites, sponsors, legal teams, and internal stakeholders, you will help ensure efficient contract execution while balancing compliance, risk management, and study timelines.

Position Summary

The Senior Site Contract Specialist is responsible for drafting, reviewing, negotiating, and finalizing clinical trial agreements and investigator budgets in accordance with company, client, and local requirements. This role serves as a key partner in the site activation process, ensuring contractual activities are completed efficiently while identifying and mitigating legal, financial, and operational risks. The position requires strong negotiation skills, attention to detail, and the ability to collaborate across multiple functions to support study start-up objectives.

Key Responsibilities:

Draft, review, negotiate, and finalize agreements with investigative sites in accordance with local regulations, company policies, and client requirements.
Lead investigators grant and budget negotiations within approved parameters and escalation pathways.
Ensure compliance with contractual processes, negotiation guidelines, approval requirements, and client expectations.
Assess and escalate legal, financial, and operational risks as appropriate.
Provide recommendations and alternative solutions to facilitate contract negotiations and issue resolution.
Collaborate with internal stakeholders to align contractual activities with site activation timelines and study objectives.
Support achievement of study start-up and site activation milestones through efficient contract execution.
Ensure adherence to budgetary guidance, templates, and contractual standards.
Maintain accurate documentation and tracking of contractual activities within company systems.
Facilitate effective communication among study sites, sponsors, legal teams, and operational stakeholders.
Support continuous process improvement initiatives and promote best practices in contract management.
Ensure contractual risks and outstanding issues are proactively identified, reviewed, and managed.

Minimum Qualifications:

Bachelor’s degree or equivalent combination of education, training, and relevant experience.
Understanding of clinical research, site activation processes, and contract management principles.

Experience:

Relevant experience in contract negotiation, site contracting, clinical operations, legal support, or related functions within a pharmaceutical, biotechnology, CRO, or healthcare environment.
Candidates will be considered based on their experience, qualifications, and demonstrated expertise in clinical trial agreements, budget negotiations, and risk assessment.

Preferred Skills & Competencies:

Understanding of contract law principles and regulations impacting clinical trial agreements.
Knowledge of investigator grant and budget negotiation processes.
Understanding of business, financial, and operational considerations related to clinical research contracts.
Strong negotiation, analytical, and problem-solving skills.
Excellent attention to detail and risk assessment capabilities.
Effective written and verbal communication skills in English.
Strong organizational and time management skills.
Ability to manage multiple priorities and deadlines in a dynamic environment.
Ability to work independently and collaboratively across cross-functional teams.
Customer-focused approach to communication, issue resolution, and stakeholder management.
Proficiency with Microsoft Office and contract management systems.

Working Conditions & Environment

Work is performed in an office and/or home-based environment with exposure to standard office equipment and technology.

May collaborate with global teams across multiple time zones.

Postulate ahora

Refiná tu búsqueda

sr site contract specialist empleos en buenos aires, b

Sr. Site Contracts Associate, IQVIA Biotech

Sr. Safety Specialist

More jobs to discover

Quiero recibir la alerta de empleo más reciente para sr site contract specialist en buenos aires, b

Explorar empleos en más ubicaciones

Join Us as a Sr Site Contract Specialist

Make an Impact at the Forefront of Innovation

Position Summary

Key Responsibilities:

Draft, review, negotiate, and finalize agreements with investigative sites in accordance with local regulations, company policies, and client requirements.

Lead investigators grant and budget negotiations within approved parameters and escalation pathways.

Ensure compliance with contractual processes, negotiation guidelines, approval requirements, and client expectations.

Assess and escalate legal, financial, and operational risks as appropriate.

Provide recommendations and alternative solutions to facilitate contract negotiations and issue resolution.

Collaborate with internal stakeholders to align contractual activities with site activation timelines and study objectives.

Support achievement of study start-up and site activation milestones through efficient contract execution.

Ensure adherence to budgetary guidance, templates, and contractual standards.

Maintain accurate documentation and tracking of contractual activities within company systems.

Facilitate effective communication among study sites, sponsors, legal teams, and operational stakeholders.

Support continuous process improvement initiatives and promote best practices in contract management.

Ensure contractual risks and outstanding issues are proactively identified, reviewed, and managed.

Minimum Qualifications:

Bachelor’s degree or equivalent combination of education, training, and relevant experience.

Understanding of clinical research, site activation processes, and contract management principles.

Experience:

Relevant experience in contract negotiation, site contracting, clinical operations, legal support, or related functions within a pharmaceutical, biotechnology, CRO, or healthcare environment.

Candidates will be considered based on their experience, qualifications, and demonstrated expertise in clinical trial agreements, budget negotiations, and risk assessment.

Preferred Skills & Competencies:

Understanding of contract law principles and regulations impacting clinical trial agreements.

Knowledge of investigator grant and budget negotiation processes.

Understanding of business, financial, and operational considerations related to clinical research contracts.

Strong negotiation, analytical, and problem-solving skills.

Excellent attention to detail and risk assessment capabilities.

Effective written and verbal communication skills in English.

Strong organizational and time management skills.

Ability to manage multiple priorities and deadlines in a dynamic environment.

Ability to work independently and collaboratively across cross-functional teams.

Customer-focused approach to communication, issue resolution, and stakeholder management.

Proficiency with Microsoft Office and contract management systems.

Working Conditions & Environment

Work is performed in an office and/or home-based environment with exposure to standard office equipment and technology.

May collaborate with global teams across multiple time zones.