Clinical Research Talent in the Greater New Jersey Region

15 years

AS

Preparing regulatory documents for IRB, data collection, AE reporting, and EDC. Therapeutic areas: Oncology, Hematology, Pediatric

14 years

BS

Site initiation, trail management, CTMS management, and SAE reporting. Therapeutic area: Oncology

13 years

MPH / BSN

On-site monitoring, CRF review, source document verification, query resolution, and EDC. Therapeutic areas: Oncology, Hematology, Cardiovascular, Neurology

12 years

MS

Site initiation, interim monitoring, reviewing source documeSts, CRFs, informed consents, and close out activities. Therapeutic areas: Cardiovascular, Dermatology, Hematology

9 years

MPH

Site qualification, site management, close out visits, SAE reporting, Medidata RAVE, and CTMS

7 years

MS

Site initiation, routine monitoring, close-out, ICF development, eTMF reconciliation, and source data verification

7 years

AS

Monitoring Phase I-IV trials, site qualification, initiation, close-out, and tracking SAEs. Therapeutic areas: Cardiovascular, CNS, Endocrinology

6 years

BS

Site initiation, monitoring, close-outs, TMF maintenance, and CRF review. Therapeutic areas: Cardiovascular, CNS, Respiratory, Dermatology, Oncology

5 years

BS

Study initiation, monitoring, close-out, patient enrollment, data collection, and CRF completion. Therapeutic areas: Oncology, Medical Device

1 year

BS

Resolving data queries, data collection, and scheduling patient tests. Therapeutic area: Oncology