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Quintiles

Senior Clinical Research Associate (Sr.CRA)

PURPOSE

Conduct monitoring visits at assigned sites for protocols that are complex and/or require knowledge in advanced therapeutic areas. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.

RESPONSIBILITIES

Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.

Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.

Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.

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Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Project Manager (CPM), Clinical Research Specialist (CRS) and/or line manager.

Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.

Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

Act as a mentor for clinical staff including conducting co-monitoring and training visits.

May provide assistance to the Clinical Project Manager and/or CRS with design of study tools, documents and processes.

All responsibilities are essential to job functions unless noted as non-essential (N).

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

In depth therapeutic and protocol knowledge as provided in company training

Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer

Strong written and verbal communication skills including good command of English language

Excellent organizational and problem-solving skills

Effective time management skills

Ability to manage competing priorities

Ability to establish and maintain effective working relationships with coworkers, managers and clients

Job ID: 5c2f3b0bc95be719e86b4590cccfa0ab
Employment Type: Other

This job is no longer available.

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