Senior Clinical Trials Associate

Worldwide; Buenos Aires; Híbrido; ARS 90.547.000 - 135.820.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking a Senior Clinical Trials Associate to provide administrative and project tracking support to the clinical project team. You will arrange access, audit documents, manage Investigator Site Files, and ensure accurate trial master file versioning.

The role requires a degree or equivalent experience with at least two years in a related field, plus strong English skills and Spanish fluency for Argentina.

Formación

• Degree level qualification or equivalent experience plus a minimum of two years’ experience in a related role.
• Excellent written and verbal English is required; Spanish language fluency is expected for Argentina.
• Strong interpersonal, organizational and problem-solving abilities.

Responsabilidades

• Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.).
• Maintain and quality audit to assure the most recent revisions of documents are on project portals.
• Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File.
• Maintain version and quality control of project documentation and submit to trial master file.
• Assist with tracking and maintenance of project related information, including site medical question and answer log.
• Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management.

Conocimientos

Excellent written English

Verbal English

Spanish language fluency

Interpersonal skills

Attention to detail

Organizational skills

Problem-solving skills

Educación

Degree level qualification or equivalent experience

Descripción del empleo

## Senior Clinical Trials AssociateApply: Remote: Buenos Aires, Argentina: Virtual Mexico: Full time: Posted Yesterday: JR102929**Who we are**We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.**Why Worldwide**We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!**What the Senior Clinical Trials does**The Senior Clinical Trials Associate is responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.**What you will do*** Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)* Maintain and quality audit to assure the most recent revisions of documents are on project portals* Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File* Maintain version and quality control of project documentation and submit to trial master file* Assist with the tracking and maintenance of project related information, including site medical question and answer log* Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management**What you will bring to the role*** Excellent written and verbal English as well as fluency of the language of the country of location* Strong interpersonal skills* Strong attention to detail and focus on quality of work* Strong organizational and problem-solving skills**Your experience*** Degree level qualification or equivalent experience plus a minimum of two years’ experience in a related role* Skill sets and proven performance equivalent to the aboveWe love knowing that someone is going to have a better life because of the work we do.