[Skip to main content](#main-content) [OpenNash Jobs](https://jobs.opennash.com/) [Hiring report](/reports/hiring/) · [All AbbVie jobs](https://jobs.opennash.com/companies/abbvie/) · [Search jobs](/search/) AbbVie # Study Management Associate Iii In Mexico City Cdmx Jid 33821 Executive & Management Listed on AbbVie’s official careers site. Listed as of October 18, 2026. Check that it is still open and apply there. [Apply on AbbVie’s careers site →](https://careers.abbvie.com/en/job/study-management-associate-iii-in-mexico-city-cdmx-jid-33821) [OpenNash Jobs](https://jobs.opennash.com/) / [AbbVie](https://jobs.opennash.com/companies/abbvie/) / Study Management Associate Iii In Mexico City Cdmx Jid 33821 ## Job description Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. ### Job Description As a Study Management Associate III, you will be part of a dynamic, centralized study management team that is responsible for the execution of our global clinical trials and a key member of the study team. The Study Management Associate III works as an independent, contributing member of a cross-functional and global partnership to plan, execute and manage one or more Phase 0-4 clinical trials under the guidance of the Study Project Manager and SMA Manager. The Study Management Associate III works to ensure that assigned studies are executed with quality and efficiency, in accordance with timelines and budget to support broader company strategic objectives. The Study Management Associate III is expected to work in accordance with all AbbVie Ways of Working. This is a global role and may be located virtually. ### Responsibilities The Study Management Associate III is expected to work independently as a clinical study leader and contributor with appropriate support from the Study Project Manager on the following activities in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures): Study-level oversight and leadership of one or more global trials in a cross-functional environment for activities from inception through closure, connecting functional work and strategic work across the global study, including but not limited to: - Supports the Study Project Manager in strategic leadership of the cross-functional team through stakeholder engagement and influence to drive deliverables and timelines, including strategy development, meeting facilitation, and timely documentation at the study level to drive for timely execution of clinical trial(s) - Vendor management, including Request for Proposal (RFP)/initiation, selection, Scope of Work development & review, deliverable oversight, and risk management for one or more external vendors, e.g., central lab, recruitment, imaging, internal and external committees - Recruitment management, including thoughtful review of intelligence data, leadership, cross-functional development, and execution of recruitment strategies and mitigation planning on a global scale from country feasibility through subject recruitment and retention - Leadership of assigned meetings (cross-functional (internal), vendor, and/or investigator) and provision of regular updates on study status, e.g., agenda development, minutes curation and filing. - Ensure inspection readiness and participate in related activities. Risk identification, mitigation, and management, including timely issue review, escalation, and management to support trend analysis and risk prevention. Co-development and management (review, revision, tracking and filing) of study materials, including but not limited to: - Protocols, regulatory submissions, patient reported outcome measures, study execution plan, informed consent, site budgets and agreements, clinical study report, training materials, newsletters, presentations for various stakeholders o CTMS and eTMF management to ensure compliance/inspection readiness, support trend analyses and support timelines o EDC, IRT, and ePRO, which includes review of design specifications, participation in user acceptance testing, and contribution to development and review of associated plans and key risk indicators, as well as system management activities like access support, query resolution, and oversight. Management of investigational product and other associated study supplies. Provide engaging training to identified stakeholders as needed, e.g., study team members, vendors. Support global submission strategies. - Support process improvement initiatives or serve as a subject matter expert and/or mentor ### Qualifications - Bachelor’s Degree or OUS equivalent required - Must have at least - 4 years of progressive Pharma-related/clinical research-related experience with a high level of core and technical competencies Competent in application of standard quality procedures (SOP, ICH/GCP, Global Regulations) Experienced user of systems such as EDC, IRT, CTMS, and eTMF Strong analytical and critical thinking skills to evaluate complex issues from multiple perspectives to actively develop strategies and drive smart decision making to support acceleration of study timelines and enable a well-run study. - Excellent organizational and time management skills, strong attention to detail. Exceptional interpersonal skills with ability to communicate effectively in a clear and persuasive manner in a global setting; proficient in business/technical English-language (oral and written) Proactive, collaborative mindset Ability to work independently in a fast-paced global team environment Preferred: Exposure to study initiation through completion activities; global study exposure Additional Information ​Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​ This job is eligible to participate in our short-term incentive programs. ​ Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. ​ AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html) US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: [https://www.abbvie.com/join-us/reasonable-accommodations.html](https://www.abbvie.com/join-us/reasonable-accommodations.html) ## At a glance - Posted by the employer: Not stated - First seen by OpenNash: Oct 11, 2026 - Last checked: Oct 18, 2026 - Listed for: 7 days[Apply on AbbVie’s careers site →](https://careers.abbvie.com/en/job/study-management-associate-iii-in-mexico-city-cdmx-jid-33821) ## More jobs at AbbVie ### [Assoc Dir Director Ventures Asia Pacific In Shanghai Shanghai Jid 31896](https://jobs.opennash.com/companies/abbvie/jobs/522278c0c55a3c94ab32/) ### [Associate Director Aesthetics Ai Strategy In Irvine Ca Jid 32761](https://jobs.opennash.com/companies/abbvie/jobs/dd4e776e47fcb9a6d639/) ### [Associate Director Ami Curricula In Irvine Ca Jid 34047](https://jobs.opennash.com/companies/abbvie/jobs/415f4404d9cbf7b8d724/) ### [Associate Director Business Excellence Portfolio Strategy Aesthetics In Irvine Ca Jid 29529](https://jobs.opennash.com/companies/abbvie/jobs/f447cd668d5ce8917d61/) ### [Associate Director Category Management In Florham Park Nj Jid 30602](https://jobs.opennash.com/companies/abbvie/jobs/64a3c2f8eff34e4f145e/) ## Similar jobs at other companies ### [Ibx Critical Facilities Engineer Iii Queretaro Mexico](https://jobs.opennash.com/companies/equinix/jobs/91dce6b4515ddafceb5c/) Equinix ### [Customer Relationship Management Intern | GBS Mexico](https://jobs.opennash.com/companies/siemens/jobs/48c9aafe14d973342ae2/) Siemens ### [Toxicology Study Monitor Principal Scientist Iii](https://jobs.opennash.com/companies/novartis/jobs/bc7f074d9e02a6e8cc1c/) Novartis ### [Distributor Sales Engineer, Electrical Products (Mexico City)](https://jobs.opennash.com/companies/siemens/jobs/d8de7487964c4ddca17e/) Siemens ### [Cloud Contact Center (Amazon Connect) Consultant - Mexico](https://jobs.opennash.com/companies/accenture/jobs/d6a8046fa8e1af047d72/) Accenture OpenNash lists jobs from employers’ own careers sites and does not handle applications. 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