Site Care Partner/Lead CRA - Northeast - FSP

Parexel; Salt Lake City (UT); On-site; USD 70,000 - 110,000; Full time

Job summary

Parexel seeks a Site Care Partner in Salt Lake City to coordinate site start-up, activation, and ongoing engagement across the study lifecycle. You will collaborate with investigators, CRA teams, and vendors to ensure timely activation, robust data capture, and patient safety.

Responsibilities include site qualification, monitoring readiness, issue resolution, and maintaining strong relationships with site organizations while upholding Parexel standards and ICH-GCP guidelines.

Qualifications

• Knowledge of Good Clinical Practice/ICH Guidelines
• Proficient computer skills and ability to adapt to new technologies
• Strong communication and interpersonal skills

Responsibilities

• Site start-up and activation coordination with CRA teams and vendors
• Maintain relationships with Site Organizations and Strategic Partners
• Provide site intelligence and support to study management
• Ensure site quality and patient safety com mensurate with Parexel standards
• Support regulatory and start-up activities to achieve timely site activation
• Monitor and resolve escalated site issues related to study delivery

Skills

Good communication skills

Interpersonal skills

Willingness to travel

Computer skills

Job description

The Site Care Partner is a crucial liaison for investigative sites throughout a study's lifecycle, responsible for site start-up, activation, relationship management, recruitment, and quality assurance. This role also contributes to site selection, provides local intelligence, ensures site support, resolves issues, and collaborates with various functions to optimize communication, maintain site quality and patient safety utilizing data analytics to identify and mitigate risks.

Key Accountabilities:

Site start-up and activation

• Deploys client site strategies by qualifying and activating assigned sites

• Supports processes to optimize country & site selection activities including review and assessment of the draft potential site list and provide site qualification output for site selection

• Collaborates with key stakeholders providing country/regional level input to country outreach surveys including protocol feasibility, country Standard of Care (SOC) and medical practices (as applicable) under supervision

• Maintains a knowledge of assigned protocols

• Conducts study start-up activities at the site level including but not limited to Site Qualification, coordination of site activation checklist items, Informed Consent Form (ICF) finalization, Site Initiation Visit (SIV) as applicable, including management of issues that may compromise time to site activation

• Ensures all the site initiation activity including training per site activation checklist, collect and / complete necessary documentation/ systems needed for site activation

• Supports country specific ICF review and deployment up to Site Activation

• Ensures follow up activities’ completion post Site qualification visit and SIV to ensure site readiness for First Subject First Visit (FSFV)

• Partners with Clinical Research Associate (CRA) to ensure site monitoring readiness in anticipation of FSFV

• Responsible for relationship building and operational quality of the site

• Responsible for establishing and maintaining relationships with Site Organizations and Strategic Partners

• Provides study support on escalated site issues related to study delivery by coordinating communications and resolution efforts. (e.g., vendor, site contracts and payment issues etc.)

• Ensures the strategy and approach for Investigational Product (IP) and ancillary supplies for sites and country requirement throughout the lifecycle of the study

• Accountable for effective site recruitment planning and delivery, consistent with global and/or country plan and local targets; Jointly responsible with CRA for enrollment delivery during study conduct

• Partners with local Regulatory authorities and Study Start up teams to ensure timely completion on country / local registry up to Site Activation

Intelligence gathering

• Provides input into site recommendations via intimate understanding of country/region, sites, processes and practices, and associated site performance metrics

• Provides support to study management to define local requirements for the importation/exportation processes of the investigational medical product and ancillary supplies

Study conduct and close-out

• Reviews Site Reports and related issues

• Assures quality and consistency in the delivery of monitoring

• Supports the CRA to develop positive Investigator relationships throughout the life of the study and elevate any training or compliance concerns with Study Management

Compliance with Parexel standards

• Complies with required training curriculum

• Completes timesheets accurately as required

• Submits expense reports as required

• Updates CV as required

• Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs, and other applicable requirements

Skills:

• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements

• Must demonstrate good computer skills and be able to embrace new technologies

• Good communication, presentation, and interpersonal skills

• Ability to manage required travel

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