Job Details

ID #51282103
Estado Massachusetts
Ciudad Dedham
Full-time
Salario USD TBD TBD
Fuente Actalent
Showed 2024-03-19
Fecha 2024-03-19
Fecha tope 2024-05-18
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Clinical Trial Associate - Medical Device

Massachusetts, Dedham, 02026 Dedham USA
Aplica ya

Responsibilities

Maintain the Trial Master Files (TMF): Responsible for the on-going management of the TMF for assigned clinical trials. This is inclusive of receipt, review, QC, tracking and filing of all documents per the SOPs required within the conduct of assigned clinical trials.

Ensure all TMF documents are up to date such as 1572’s CV’s and Investigator Medical Licenses to ensure audit readiness.

Assist with the development and maintenance of tracking tools for patient recruitment, site ramp-up, monitoring visits and site payments.

Work with Clinical Operations to assist in the oversight of CROs, as appropriate, to ensure the successful conduct of clinical trials, including attending and participating in Clinical Trial Working Groups as needed.

Assist in reviewing monitoring visit reports to ensure proper conduct and oversight as needed.

Review site-specific Informed Consent Forms

Tracks site feasibility questionnaires

Assist in the planning of various meetings and events for the Clinical Operations Team

Reconcile invoices to their corresponding contracts and budget, and assist with investigator site payments.

Prepare and manages study communications including newsletters and study updates

Records, prepare and distributes meeting minutes for assigned clinical trials or as designated by the VP of Clinical Operations.

Work closely with Clinical Trial Managers to assist with preparation of all external and internal documentation for assigned trials to ensure it's completed in accordance with GCP regulatory requirements and consistent with the study protocol.

Minimum Requirements:

Three or more years’ experience as a clinical research coordinator

Medical device experience required

About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent

Maintaining an inclusive environment through persistent self-reflection

Building a culture of care, engagement, and recognition with clear outcomes

Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] (%[email protected]) for other accommodation options.

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