Initiation Clinical Research Associate I

Parexel is in the business of improving the world's health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values; Patients First, Quality, Respect, Empowerment & Accountability.

Due to an expanding portfolio, we are currently looking for an Initiation (study start up) CRA I for our team in Israel. The role is homebased but you will need to go to the office in Tel Aviv for some office based work.

This is a one year fixed term contract.

Job Purpose
An initiation Clinical Research Associate (iCRA) specializing in Pre SIV and Activation tasks will be assigned & accountable for managing and driving the strategy for the startup, Pre SIV and Activation tasks of the study. The iCRA also supports submission and approval process for the protocol amendments if applicable.

Key Accountabilities

Start-up (from site identification through site activation)

Act as Parexel's direct point of contact with assigned sites, accountable for quality and delivery during the start-up phase. Build relationships with investigators and site staff. Support on request country specific feasibility and/or site pre-qualification and qualification activities, which may include: o Preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA) and any amendments. o May conduct remote Qualification Visits (QVs). Liaison with stakeholders to understand Clinical Site Agreements (CSA) timelines. Manage country and site level TMF issues ensuring documents' First Time Quality (FTQ) as well as providing direct resolution to reported site problems. Develop strategy to configure, distribute, collect, and review and approve, high quality country specific and/or site specific documents or essential regulatory documents (Site SIV Readiness/Greenlight Documents) and any updated or amended regulatory documentation. Customize, review, and negotiate as needed, country/site specific Informed Consent Forms (ICF), translations (within parameters of country/regulatory/client requirements), and customize and negotiate any amendments. Prepare and submit IRB/IEC and MoH/RA (if applicable) application(s), resolving conflicts, determining appropriate follow up until receipt of final approval. Submit all pertinent documentation to the trial master file as per project plans/sponsor/company policy. Forecast, develop, manage, and revise plans and strategies for: o IRB/IEC and MoH / RA submission/approval,
o Site activation, Update and maintain appropriate Clinical Trial Management System (CTMS) in a timely manner. Promptly identify, use judgment and knowledge to address and resolve or escalate, any site question and/or issue, including but not limited to: potential issues or risks with site activation timelines, issues with patient recruitment strategy, deficiencies in training, data quality or integrity, study non-compliance, etc. Facilitate and support allocated sites with access to relevant study systems and ensure they are compliant with all project specific training requirements prior to study start. Actively participate in internal and/or external meetings as per project needs, Sponsor's expectations and at Manager discretion Work in a self-driven capacity, with limited need for oversight. Proactively keep manager informed about work progress and any risk or issues Maintenance (from initiation through close out) Customize, review, and negotiate as needed, country/site specific Informed Consent Forms (ICF), translations (within parameters of country/regulatory/client requirements), and customize and negotiate any amendments as needed during maintenance Prepare and submit IRB/IEC and MoH/RA (if applicable) application(s), resolving conflicts, determining appropriate follow up until receipt of final approval. Forecast, develop, manage, and revise plans and strategies for: o IRB/IEC and MoH / RA submission/approval, Submit all pertinent documentation to the trial master file as per project plans/sponsor/company policy. Overall Accountabilities from Site Identification to Close out Ensure timely and accurate completion of project goals and update of applicable trial management systems with start -up and amendments Work with team members to meet project goals, provide strategy for efficient project planning and goal completion, and encourage the support of team members where required. Update all appropriate Clinical Trial Management Systems (CTMS) on an ongoing basis including performing regular reviews of country and site level data in clinical systems (e.g. CTMS, and SIS) and ensure timely and high quality data entry compliance from sites, manage and submit all relevant documents to the Trial Master File (TMF), ensuring first time quality, and distribute study documents to site including configuration of Investigator Site Files if applicable and on-going maintenance for completeness and quality. Ensure that assigned sites are audit and inspection ready Monitor and maintain compliance with ICH-GCP and applicable international and local regulations. Show commitment and perform consistent high quality work. Maintain a positive, results-orientated work environment, building partnerships and collaborative relationships, communicating with team(s) in an open, balanced, objective manner, modeling the high performance culture values. Maintain a working knowledge of and ensure compliance with applicable ICH-GCP Guidelines, international and local regulations, Parexel SOPs, other Parexel / Sponsor training requirements and study specific procedures, plans and training. Ensure basic understanding of project scope, milestones, budgets, and strive for high quality, timely, and efficient delivery. Provide input and feedback for Performance Development Conversation(s). Proactively keep manager informed about work progress and any risks or issues. Develop expertise to become a subject matter expert. Work in a self-driven capacity, with limited need for oversight. Complete additional tasks in a timely manner (e.g. timesheets, expenses, metrics, etc.) Knowledge and Experience Atleast 2 years of Study Coordinator experience with an understanding of clinical trials methodology and terminology Education Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or other equivalent experience Skills Demonstrate strong problem-solving skills Able to take initiative and work independently, and to proactively seek guidance when necessary. Excellent presentation skills. Client focused approach to work. Ability to interact professionally within a client organization. Flexible attitude with respect to work assignments and new learning. Ability to prioritize multiple tasks and achieve project timelines; utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise. Strong ability to make appropriate decisions in ambiguous situations. Willingness to work in a matrix environment and to value the importance of teamwork. Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Trial Master File (eTMF) , and MS-Office products such as Excel and Word. Excellent interpersonal, verbal, and written communication skills. Sense of urgency in completing assigned tasks and ability to assist others to meet study/country deliverables. Excellent time management in order to meet study needs, team objectives, and department goals. Proven ability to work across cultures. Shows commitment to and performs consistently high-quality work. Ability to successfully work in a ('virtual') team environment. Act as a mentor and role model for other team members. Effectively enlist the support of team members in meeting goals. Attention to detail.
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