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Senior Clinical Research Associate (Argentina)
Remote, Argentina
We're expanding our capabilities across Latin America, and we're hiring a Senior Clinical Research Associate to support critical studies across Argentina.
As a Senior CRA you'll possess a wide-ranging and broad experience handling our most complex and advanced assignments.
Responsibilities will be dependent upon the type and timing of the program to which the Senior CRA is assigned and will, at a minimum, include start-up and study implementation activities, on‐site monitoring of clinical research studies as well as on-going site management.
Incumbents are expected to be able to manage appropriately sized or complex clinical trials, and support Clinical Trial Managers and/or Project Managers with trials as required.
An increased focus on training and mentoring junior staff members may be expected.
Responsibilities
Independently oversee all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low query levels and in acceptable Quality Assurance reports
Provide guidance at the site and project level towards audit readiness standards and support preparation for audit and required follow-up actions
Establish, update, track and maintain study specific trial management tools/systems, and status reports
Manage site start up procedures including the feasibility and recruitment of potential investigators, preparation of EC/IRB submissions, collection and review of regulatory documents, review and adaptation in Patient Informed Consents, notifications to IRB, EC and regulatory authorities, as appropriate, translation of study related documentation, organization of meetings and other tasks as instructed by the Clinical Trial Manager/Project Manager
If required, assist the negotiation of study budgets and the execution of investigator contracts under directions of Site Contract Management department/designee
Verify the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate.
Assess factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues
Independently conduct all forms of site visits, including pre-study/qualification, initiation, routine monitoring, and close-out visits, in accordance with the protocol, local laws, ICH-GCP and Precision SOPs.
Perform Monitoring Oversight Visits to assess other CRA team members.
Prepare and submit for review, accurate and timely monitoring reports from all site visits (on-site and remote)
Document activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs, Clinical Monitoring Plan/Site Management Plan and client requirements.




Support subject/patient recruitment, retention and awareness strategies.
Enter data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution
Routinely review the Investigator Site File (ISF) for accuracy, timeliness and completeness.
Reconcile contents of the ISF with the Trial Master File (TMF).
Ensure the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations
Communicate effectively and proactively with both site personnel and Precision's Project and Clinical Trial Management to relay protocol/study issues including any deviations and implement necessary actions in response to those issues
Develop and maintain good working relationship with investigators and study staff, serving as an ambassador to promote Precision's high quality and professional image
Perform investigational product (IP) inventory, reconciliation and review storage and security.
Verify the IP has been dispensed and administered to subjects/patients according to the protocol.
Verify issues or risks associated with blinded or randomized information related to IP.
Apply knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned
Perform data review activities, including remote EDC CRF and patient profiles review, query resolution, and assist data management and clinical data quality personnel to resolve data discrepancies
Identify and process Serious Adverse Events according to the procedures defined by the study team.
Also demonstrate a full understanding of the SAE reporting process
Identify site risks and elevate those to Clinical Trial Manager/Project Manager with suggested contingencies.
Own the timely and appropriate resolution of the risk with oversight from project team
Prepare for and attend Investigator Meetings and/or sponsor face‐to‐face meetings.
Participate in integral clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attend clinical training sessions according to the project specific requirements.
May prepare or assist in preparation of study‐specific presentations/training materials and tools
Assist the team managers in the preparation and review of protocols and other study documentation
Support the design and development of CRFs and clinical trial documents as they pertain to clinical monitoring activities (i.e. operating manuals,



monitoring guidelines, etc.)
Assist with review of clinical study reports
Function as a mentor, assisting with the training and developing of new employees and junior monitors
Interact with client, participate in proposal activities, including development and client presentations
Initiate payment requests for investigators
Travel as necessary according to project needs
Other job duties as assigned
Qualifications
4-year college degree or equivalent experience in a scientific or healthcare discipline
5 years or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies
Significant site management experience or equivalent experience in clinical research
Ability to communicate both verbally and in writing at the English proficiently (Professional level)
Preferred Education & Experience
Experience monitoring in rare and complex therapeutic areas
Experience monitoring EDC trials and EHR records
Experience in biopharma or relevant therapeutic area
Relevant site start‐up (feasibility, contract negotiations, submissions) experience for the country
Ability to monitor study sites, with supervision, according to protocol monitoring guidelines, SOPs, GCP and ICH guidelines
Ability to resolve project related problems and prioritize workload to meet deadlines with oversight from management.
Can assist junior CRAs in problem resolution
Ability to travel overnight.
Up to 60% travel on average, based on regional requirements.
International travel as needed
Select opportunities require Oncology experience preferably in early phases
Exhibits self‐motivation and is able to work and plan independently as well as in a team environment.
Understands clinical trials methodology, including a working knowledge of protocols and indications being studied.
Demonstrated ability to conduct formal presentations to a wide variety of audiences including colleagues, investigative staff, and clients with a high level of proficiency.
Demonstrated focus on continuous improvement, including the ability to make proactive assessments on how to make processes more efficient and people more effective.
Equal Employment Opportunity Statement
Precision Medicine Group is an Equal Opportunity Employer.
Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
Accommodation for Applicants with Disabilities
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at .
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📌 Senior Clinical Research Associate (Argentina) (Chubut)
🏢 Precision For Medicine
📍 Chubut