Buenos Aires, Buenos Aires, Argentina
Full time
R

Chevron – Project Manager (Global Business Services)

Chevron's Integral Business Services (GBS) organization located in Buenos Aires is accepting applications for the position of Project Manager. Successful candidates will join the IT Organization, a multifunction service center with more than 1800 employees that deliver business services and solutions to the corporation across the globe.

We are seeking passionate individuals who exemplify high‑performing behaviors and share our vision of bringing innovative solutions and efficient project management practices to our organization. The Project Manager will be responsible for planning, executing, and finalizing projects in the SAP landscape according to strict deadlines and within budget. This role requires a strategic thinker who can manage multiple projects, coordinate team members, and communicate effectively with stakeholders.

- Define project scope, objectives, and deliverables.
- Allocate tasks and coordinate team members.
- Estimate costs and ensure the project stays within budget.
- Identify issues and develop mitigation strategies.
- Keep stakeholders informed with regular updates and reports.
- Ensure project deliverables meet required standards.
- Complete project documentation and evaluations.

Requirements

- Bachelor's degree in an IT or business‑related discipline.
- 5‑10 years of project management experience, preferably with ERP implementation and support experience.
- Current PMP Certification or similar.
- Proficient use of project management tools such as Microsoft Project or ADO.
- Strong facilitation and stakeholder engagement experience.
- Highly proficient in English.




- Strong verbal and written communication skills.
- Organizational and problem‑solving skills to manage multiple tasks, prioritize effectively, and adapt to changing project conditions.
- Ability to work in a multicultural and diverse environment.

Preferred Qualifications

- Master's degree preferred.
- Agile certification(s).
- Strong understanding of Agile frameworks.

Relocation Options

Relocation may be considered.

International Considerations

Expatriate assignments will not be considered. Chevron regrets that it is unable to sponsor employment Visas or consider individuals on time‑limited Visa status for this position. Chevron participates in E‑Verify in certain locations as required by law.

About Chevron

Chevron is a leading integrated energy company. It explores, produces, transports crude oil and natural gas; refines, markets and distributes transportation fuels and lubricants; manufactures and sells petrochemicals and additives; generates power; and develops and deploys technologies that enhance business value in every aspect of its operations. It is based in Houston, Texas.

Equal Opportunity

Chevron is an Equal Opportunity / Affimative Action employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation,



gender identity, national origin, disability or protected veteran status, or other status protected by law or regulation.

Diverse, Inclusive Culture

Indero is a contract research organization (CRO) specialized in dermatology and Rheumatology. Based in Montreal, Indero continues to grow and expand in North America and Europe. It offers a stimulating work environment, attractive advancement opportunities, and benefits such as flexible work schedule, home‑based position, and ongoing learning and development.

Indero is committed to providing equitable treatment and equal opportunity to all individuals. It will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request. Indero only accepts applicants who can legally work in Argentina.

Education

- B.Sc. in a related field of study to clinical research.

Experience

- At least 3 years of experience in a similar role, including activities related to management of clinical studies in the pharmaceutical, biotechnology and/or CRO industry.
- At least 2 years experience coordinating activities related clinical trial management.

Knowledge and Skills

- Excellent knowledge of GCP and ICH standards, FDA and Canadian regulations.
- Excellent knowledge of Microsoft Office suite.
- Excellent oral and written skills in English; French is an asset.
- Excellent communication skills.
- Ability to work in a team environment and establish good relationships with colleagues and sponsors.
- Good problem‑solving abilities.
- Good organizational skills.
- Strong ability to carry out different projec

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