Research Nurses' Services

With its exclusive pool of technicians, research nurses and site coordinators, Mission TEC provides unique resources to organizations in need of skilled personnel to manage field-based Clinical Research operations.

nurse at work
  • Competent => highly qualified, experienced and committed staff
  • Flexible => part-time or full-time solutions
  • Widespread =>  2-hr radius presence across the whole country

Since its establishment in 2002, Mission TEC covered a wide range of indications. Our staff is accustomed to operate in a large variety of working environments: according to clients’ requirements, we can either fit our ressources within existing team structures to offer additional support, or use our teams to drive projects at sites without existing research infrastructure. Mission TEC ensures high quality subject/patient care, maximizes participants’ recruitment and preserves integrity of trial data under all circumstances.
At patient's home or at the hospital,
Mission TEC's Clinical Research expertise fully complies with ICH as well as EU directives, and covers all aspects of field-based operations:

Our sphere of activities:

 

For the administrative assistant:

Patient planning management, update of binders, fax, mails...

For the investigator

Patient selection, research of source data, (e)CRF and database completion, queries management, AE/SAE declaration, co-monitoring with sponsor's CRAs. 

For the laboratory

Sample kits management, shipping and carrier management...

For the patients

Management and administration of patient questionnaires, home care services...

For the nurse

Samples, injections, vital signs, product training to hospital team...

  • Subject-centered services

    • Subjects / patients recruitment
    • Patients’ training and therapeutic education
    • Administration of study questionnaires
    • ePRO
    • Home visits
    • Nursing care
  • Support to Investigators

    • Evaluation of patients’ vital signs and demographic data
    • Support to surgeon (mainly for medical device trial)
    • Administration of study drug (infusion, injection, topical or oral)
    • Monitoring of concomitant medications
    • Biocaptors management (ECGs, blood pressure monitors…)
    • Collection and processing of biological specimens (blood, urine, antibodies… / PK & PD)
    • Maintenance of regulatory files 
    • CRF and eCRF completion

  • Pharmacy Services

    • Administration of investigational medicinal product(s)
    • Liaison with central laboratories
    • Disposal of medical waste
    • Related supplies delivery

 

  • Project Management Services

    • Regulatory file submissions
    • Protocol/study procedures
    • Identification and training of local clinicians
    • Contract and vendor management
    • Liaison with Investigators and Sponsor
    • Visits with the Sponsor’s CRA
    • Data clarification forms and queries management
    • Data storage according to ICH/GCP