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Actalent Clinical Research Coordinator in Boston, Massachusetts

Actively looking to hire a Senior Clinical Research Coordinator to join a large CRO ON A PART TIME BASIS (20 hours a week) at the site level to help with clinical trials! This is a Monday to Friday; no weekends or holidays! Must be reliable and comfortable going onsite 3 days a week. This role is located in Boston, MA. Must have experience with EMR/EDC data entry and highly proficient in protocol comprehension, patient communication, and prescreening/scheduling patients.

Duties:

  • Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and SOPs

  • Independently coordinate assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.

  • Apply project management concepts to manage risk and improve quality in the conduct of a clinical research study

  • Develop, coordinate, and implement research and administrative strategies to successfully manage assigned protocols.

  • Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.

  • Apply good documentation practices when collecting and correcting data, transferring data to sponsor/CRO data capture systems and resolving queries

  • Maintain confidentiality of patient protected health information, sponsor confidential information and confidential information

  • Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely manner

  • Create, collect and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations and IRB requirements.

  • Evaluate potential subjects for participation in clinical trials including phone and in person pre-screens

  • Create and execute recruitment strategies defined by Clinical Research Team

Qualiications:

  • 2+ years of Clinical Research Coordinator Experience

  • Experience with EDC Data Entry and patient recruitment

  • Can commit to 20 hours a week! - 2.5 days on site

  • Reliable

    About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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