Amalia Suarez
Tampa
Summary
Resourceful Clinical Research Coordinator with strong organizational skills and detail-oriented team player. Ability to handle multiple projects simultaneously with a high degree of accuracy.
Overview
5
5
years of professional experience
1
1
Certification
Work History
Clinical Research Coordinator
Avita Clinical Research
01.2020 - Current
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Collected data and followed research protocols, operations manuals and case report form requirements.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
- Followed informed consent processes and maintained records.
- Gathered, processed and shipped lab specimens.
- Quickly learned new skills and applied them to daily tasks, improving efficiency and productivity.
- Maintained energy and enthusiasm in fast-paced environment.
- Proved successful working within tight deadlines and fast-paced atmosphere.
- Used critical thinking to break down problems, evaluate solutions and make decisions.
- Offered friendly and efficient service to customers, handled challenging situations with ease.
- Worked flexible hours; night, weekend, and holiday shifts.
Clinical Research Assistant
Avita Clinical Research
07.2019 - 01.2020
- Managed updates and input for patient information database.
- Assisted with research protocol development.
- Collected data and followed research protocols, operations manuals and case report form requirements.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Gathered, processed and shipped lab specimens.
- Collected, evaluated and modeled collected data.
- Performed clerical duties, such as word processing, data entry, answering phones and filing.
- Collected and documented patient medical information such as blood pressure and weight.
- Educated patients regarding all facets of clinical study participation.
Education
High School -
IPU Carlos Perez
Havana, Cuba06.2018
Skills
- Complex Problem-Solving
- Study Coordination
- Specimen Handling
- Medication Dispensing
- Lab Specimens and Collections
- Participation Reviews
- Records Maintenance
- Medication Side Effect Knowledge
- Informed Consent
- Creative Thinking
- Bilingual (English/Spanish)
- Database Organization
Certification
Good Clinical Practice Certification
IATA Certification
High School Diploma
Canfield Photography
Medidata Rave
RealTime CTMS
eCaselink
C-SSRS
Signant Health
TrialManager
eCOA
InvestigatorSpace
Lifesphere
CardioCore
LabCorp
VANDA
LabConnect
Medpace
Languages
Spanish
Native or Bilingual
English
Native or Bilingual
Additional Information
Study Coordinating History
- A multicenter, randomized, double-blind, placebo-controlled phase III study to assess the efficacy of XXXXX relieving symptoms of gastroparesis.
- Motion Syros: A randomized, double-blind, placebo-controlled study to investigate the efficacy of XXXXX in subjects affected by motion sickness during travel.
- A randomized, double-blind, placebo-controlled phase II study to evaluate efficacy, pharmacokinetics, and safety of multiple intravenous doses of XXXXX in adults with Atopic Dermatitis.
- A phase 2b, randomized, double-blind, placebo-controlled, parallel-group study to evaluate the efficacy and safety of XXXXX in adult patients with non-responsive celiac disease as an adjunct to a gluten-free diet.
- A phase 2 randomized, double-blind, placebo-controlled, parallel-group study of the safety and efficacy of XXXXX administered orally to patients with gastroparesis.
- A phase 2b, randomized, placebo-controlled, multicenter study to evaluate the safety and efficacy of XXXXX versus Placebo in Gout Patients.
- Motion Delos: An open-label study to investigate the safety and efficacy of XXXXX in participants affected by motion sickness during travel.
- A randomized, double-blind, placebo-controlled, efficacy study of the XXXXX receptor antagonist XXXXX in patients with Atopic Dermatitis.
- A 12-week, single-blind, placebo-controlled randomized study to evaluate the safety, tolerability, and physiological regulation of an amino acid food product, XXXXX, in subjects with mild to moderate hepatic insufficiency.
- A phase II, randomized, double-blind, placebo-controlled study of XXXXX in patients with moderate to severe Hidradenitis Suppurativa.
- A phase II, randomized, double-blind, placebo-controlled study of XXXXX in patients with moderate to severe Atopic Dermatitis.
Timeline
Clinical Research Coordinator
Avita Clinical Research
01.2020 - Current
Clinical Research Assistant
Avita Clinical Research
07.2019 - 01.2020
High School -
IPU Carlos Perez