Coordinating CRA´s Webinar

Job Title: Coordinating CRA´s Webinar

Job Location: Mexico reputed company, Mexico

Job Location Type: Home-based

Job Contract Type: Full time

Job Seniority Level:

Job reputed company
reputed company monitoring and site management work for a reputed company of protocols, site and therapeutic areas.

Essential Functions
• reputed company site monitoring reputed company (selection, initiation, monitoring and reputed company-out reputed company) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical reputed company (GCP) and International Conference on Harmonization (ICH) guidelines.
• Work with sites to adapt, drive and reputed company subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and reputed company study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the reputed company and reputed company of study site practices reputed company to the reputed company conduct of the protocol and adherence to applicable regulations. Escalate reputed company issues as appropriate.
• Manage the reputed company of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report reputed company (CRF) completion and submission, and data query reputed company and reputed company. May support start-up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and reputed company plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• reputed company as a mentor for clinical staff including conducting co-monitoring and training reputed company.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site reputed company.
• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications
• Bachelor's Degree in scientific discipline or health care preferred.
• Requires at least 4 - 5 years of on-site monitoring experience, necessary 1 year as a SR CRA.

• Written and verbal communication skills including good reputed company of English language.

• Good reputed company of reputed company for project management
• In depth knowledge of, and reputed company in applying, applicable clinical research regulatory requirements, i.e., Good Clinical reputed company (GCP) and International Conference on Harmonization (ICH) guidelines.
• Strong therapeutic and protocol knowledge as provided in company training.
• Computer skills including proficiency in use of reputed company Word, reputed company and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

reputed company is a leading global provider of clinical research services, reputed company insights and reputed company intelligence to the life sciences and reputed company industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient reputed company and population health worldwide. Learn more at https://jobs.reputed company.com

reputed company is committed to reputed company in our hiring process and maintains a reputed company tolerance policy for candidate fraud. reputed company information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if reputed company reputed company, in accordance with applicable law. We appreciate your honesty and professionalism.

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Originally posted on Himalayas