Sr. CRA - Clinical Research Associate

Sr CRA

Responsibilities:

Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.

Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.

Gains an in-depth understanding of the study protocol and related procedures.

Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.

Participates & provides inputs on site selection and validation activities.

Performs remote and on-site monitoring & oversight activities using various tools to ensure: o Data generated at site are complete, accurate and unbiased. o Subjects' right, safety and well-being are protected.

Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner.

Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.

Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.

Identifies, assesses and resolves site performance, quality or compliance problems and escalates per defined CRA Escalation Pathway as appropriate in collaboration with CRA-Manager, CRM, TA Head and CRD as needed.

Works in partnership internally with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites.

Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.

Contributes strongly to CRA team knowledge by acting as process Subject Matter Expert (SME), sharing best practices, making recommendations for continuous improvement and providing training as appropriate/required.

Supports and/or leads audit/inspection activities as needed.

Following the country strategy defined by CRD and CRA-Manager, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilities.

Mentors / buddies junior CRAs on process/study requirements and performs co-monitoring visits where appropriate.

Could perform Quality control visits if delegated by other roles and trained appropriately.

Core Competency Expectations:

Fluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively.

Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.

Excellent understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines.

Demonstrated ability to mentor/lead.

Hands on knowledge of Good Documentation Practices.

Proven Skills in Site Management including independent management of site performance and patient recruitment.

Demonstrated high level of monitoring skill with independent professional judgment.

Good IT skills (Use of MS office, use of various clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices

Ability to understand and analyze data/metrics and act appropriately, also in a virtual environment.

Experience with conducting site motivational visit designed to boost site enrollment.

Capable of managing complex issues, works in a solution-oriented manner.

Performs root cause analysis and implements preventative and corrective action.

Capable of mentoring junior CRAs on process/study requirements and is able to perform co-monitoring visits where appropriate.

Behavioral Competency Expectations:

Demonstrates commitment to Customer focus.

Works with high quality and compliance mind-set.

Effective time management, organizational and interpersonal skills, conflict management, problem solving skills.

Able to work highly independently across multiple protocols, sites and therapy areas.

High sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment.

Works effectively in a matrix multicultural environment. Ability to establish and maintain culturally sensitive working relationships.

Positive mindset, growth mindset, capable of working independently and being self-driven.

Demonstrates and projects professional demeanor and communication consistent with organizational policies and practices.

Experience and Educational Requirements:

Bachelor's degree (or above) with at least 4 years of direct site management (monitoring) experience in a bio / pharma / CRO.

7 years of relevant experience in the healthcare field, including at least 4 years of direct site management (monitoring) experience in bio / pharma / CRO.

Required Skills:

Adaptability, Clinical Site Management, Clinical Trial Agreements (CTA), Clinical Trial Compliance, Clinical Trial Documentation, Clinical Trial Management, Clinical Trial Planning, Clinical Trials Monitoring, Clinical Trials Operations, Competency Management, Conflict Management, Cross-Cultural Awareness, Cultural Awareness, Customer Centricity, Decision Making, Document Management, Growth Mindset, ICH GCP Guidelines, Matrix Management, Multitasking, Patient Recruitment, Product Information, Regulatory Compliance, Relationship Building {+ 6 more}

Preferred Skills: