Clinical Research Associate Ii

Clinical Research Associate Ii
Empresa:

*Nombre Oculto*


Detalles de la oferta

Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all stakeholders across the clinical research community with an emphasis on ethics, compliance, and innovation.Job Title: Clinical Research Associate IILocation: Remote (Europe - Spain)Function: Clinical OperationsDESCRIPTION:ESSENTIAL DUTIES AND RESPONSIBILITIES:Primary point of contact for site personnel during the life cycle of clinical trials. This includes study start-up support, site activation, trial conduct, and closeout of a clinical trial.Ability to identify protocol deviations and pharmacovigilance issues that might affect data accuracy or patient safety.Conduct site qualification, site initiation, routine site monitoring, and closeout visits (remote and onsite), Central monitoring in compliance with study protocol and ICH-GCP.Expert documentation of monitoring priorities/activities via site visit confirmation and follow-up letters, monitoring visit reports, and any trial associated logs.Oversees conduct trials by reviewing study data listings, vendor dashboards, and CTMS issues/actions documentation to identify trends, errors, and any potential breaches that can impact data integrity.Ability to present essential functions of the CRA role in Bid Defenses, Investigator Meetings, and Sponsor Face to Face meetings.Assists the Global Project Lead in identification of out-of-scope activities.Basic understanding of assigned project scope, milestones, and budget, and manages site-level activities to ensure project deliverables are met.Provides support to the CTM and Global project lead in negotiation of site budgets and contracts.EDUCATION AND EXPERIENCE REQUIRED:Years of experience and preferred education.PREFERRED SKILLS:IT skills, Management skills, etc.COMPENSATION & BENEFITS:Sitero proudly offers an impressive compensation package and benefits, including a competitive salary, Variable pay, paid time off, and healthcare and retirement benefits.EMPLOYMENT TYPE:Full Time, PermanentCOMMITMENTS:Standard Hours 40 hours per week, one hour lunch, Monday - Friday. Additional hours as needed. Willing to work in shifts as and when needed.DISCLAIMER:Sitero is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.#J-18808-Ljbffr


Fuente: Jobtome_Ppc

Requisitos

Clinical Research Associate Ii
Empresa:

*Nombre Oculto*


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