Associate Clinical Research Specialist Jobs in Maine

Experience in clinical study management required.

Manages Trial Management Filing (TMF) system, including document inspection, filing, and auditing.

Serves as key facilitator and liaison for shipping, receiving, and management of study devices.

Ability to constructively interact directly with senior management teams.

Recognition of work, respect, and our multicultural community are key aspects of the employee experience and contribute to our continued success.

Manages study and site materials, including, but not limited to study binders, study trackers, training documentation.

2+ years experience with a documentation for regulatory compliance of medical devices, clinical research, project management preferred

All training related to the quality management system is done in accordance to the Training Management Process.

Medical writer qualifications or Certified Research Associate a plus

Experience with both qualitative and quantitative research a plus

Strong collaborative and teamwork skills

We provide a flexible work environment to offer work/life balance