Accomplished Radiologic Technologist with over 12 years' experience seeking to secure a position with a respected organization. Highly skilled in producing high quality diagnostic images, comforting patients and delivering clinical instruction to staff and students. Demonstrated leadership skills which guide teams towards success and strengthen relationships with patients and physicians.
1. A multicenter, randomized, double-blinded, placebo-controlled, parallel group study of CNTO136 (sirukumab), a human anti-IL-6 monoclonal antibody, administered subcutaneously, in subjects with active rheumatoid arthritis despite anti-TNF therapy.
2. A multicenter, parallel-group study of long-term safety and efficacy of CNTO136 (sirukumab) for rheumatoid arthritis in subjects completing treatment in studies CNTO136ARA3002 (SIRROUND-D) and CNTO136ARA3003 (SIRROUND-T).
3. A multicenter, randomized, double-blinded, placebo-controlled, parallel group study of CNTO136 (sirukumab) administered subcutaneously as monotherapy compared with adalimumab monotherapy, in subjects with active rheumatoid arthritis.
4. A phase 3, randomized, double-blind, placebo-controlled, study of the efficacy and safety of 2 doses of tofacitinib (CP-690,550) in subjects with active psoriatic arthritis and an inadequate response to at least one TNF inhibitor.
5. A phase 3, randomized, double-blind, placebo-controlled study of the efficacy and safety of 2 doses of tofacitinib (CP-690,550) or adalimumab in subjects with active psoriatic arthritis.
6. A long term, open label extension study of tofacitinib (CP-690,550) for the treatment of psoriatic arthritis.
7. A randomized, double-blind, placebo-and active-controlled, phase 3 study evaluating the efficacy and safety of baricitinib in patients with moderately to severely active rheumatoid arthritis who have had an inadequate response to methotrexate and therapy.
8. A randomized, double-blind, placebo-and active-controlled, phase 3 study evaluating the efficacy and safety of baricitinib (LY3009104) in patients with moderately to severely active rheumatoid arthritis who have had limited or no treatment with disease-modifying antirheumatic drugs.
9. A phase 3, multicenter study to evaluate the long-term safety and efficacy of baricitinib in patients with rheumatoid arthritis.
10. A randomized, double-blinded, placebo-controlled, phase-2 study to investigate the safety and efficacy of ABT-494 given with methotrexate (MTX) in subjects with moderately to severely active rheumatoid arthritis (RA) who have had an inadequate response or tolerance to anti-TNF biologic therapy.
11. Phase 2 study, multicenter, open-label extension (OLE) study in rheumatoid arthritis subjects who have completed a preceding phase 2 randomized controlled trial (RCT) with ABT-494.
12. A phase 2A, 4-week, double-blind, proof-of-concept efficacy and safety study of CC-292 vs. placebo as co-therapy with methotrexate in active rheumatoid arthritis.
13. Gs-Us-417-0301-In Patients With Rheumatoid Arthritis. "Finch 1". Gilead/Galapagos
14. Gs-Us-417-0302-In Patients With Rheumatoid Arthritis. "Finch 2". Gilead/Galapagos
15. Gs-Us-417-0303-In Patients With Rheumatoid Arthritis. "Finch 3". Gilead/Galapagos
16. Gs-Us-417-0304-In Patients With Rheumatoid Arthritis. "Finch 4". Gilead/Galapagos
17. Im006-016- In Patients With Rheumatoid Arthritis. Bristol-Myers Squibb (Bms)
18. Cain457fus01- In Patients With Psoriatic Arthritis. Novartis
19. M13-538- In Patients with rheumatoid arthritis who have completed a preceding phase 2 Rct with Abt-494. Open-label extension study "balance". Abbvie
20. Ms200527-0018- In patients with systemic lupus erthyematosus (Sle) "Btki-Sle". Emd Serono Research & Development Institute, Inc.
21. M16-063- A phase 2 study to investigate the safety and efficacy of Abbv-105 given alone or in combination with Upadacitinib (Abbv-599 combination) with a background of conventional synthetic dmards in subjects with active rheumatoid arthritis with inadequate response or intolerance to biologic dmards.
22. M15-998- A phase 3, randomized, double-blind study comparing Isankizumab to placebo in subjects with active psoriatic arthritis including those who have a history of inadequate response or intolerance to biologic therapy (LES).
23. M16-011- A phase 3, randomized, double-blind, study comparing Isankizumabto placebo in subjects with active psoriatic arthritis (Psa) who have a history of inadequate response to or intolerance to at least one disease modifying anti-rheumatic drug (Dmard) therapy.
24. M16-852- Giant cell arteritis: Phase 3 safety and efficacy study of Upadacitinib in subjects with Giant Cell Arteritis.
25. I4v-Mc-Jaia- A randomized, double-blind, placebo-controlled, parallel-group, phase 3 study of Baricitinib in patients with systemic lupus erythematosus.
26. I4v-Mc-Jaja- A randomized, active-controlled, parallel-group, phase 3b/4 study of baricitinib in patients with rheumatoid arthritis.
27. M19-130- A phase 2 study to investigate the safety and efficacy of Abbv-105 and Upadacitinib given alone or in combination (Abbv-599 combination) in subjects with moderately to severely active systemic lupus erythematosus.
28. As0006-Phase 3, multicenter, randomized, placebo-controlled,double-blind study to evaluate efficacy and safety of certolizumab pegol in subjects with active axial spondyloarthritis (Axspa) without xray evidence of ankylosing spondylitis (As) and objective signs of inflammation.
29 . Im101-567- A randomized, head to head, single-blinded study to assess changes in the immune profile in response to treatment with subcutaneous abatacept in combination with methotrexate vs. subcutaneous adalimumab in combination with methotrexate in adults with early rheumatoid arthritis who are naive to biologic disease-modifying antirheumatic drugs.
30. Im014-029- A randomized, placebo-controlled, double-blind, multicenter study to assess the efficacy and safety of Branebrutinib treatment in subjects with active systemic lupus erythematosus or primary sjogren's syndrome, and Branebrutinib treatment alone and in combination with Abatacept in subjects with active rheumatoid arthritis.