Julia AlJumaily Email & Phone Number | I am a skilled and experienced clinical research professional with a proven record of accomplishments ensuring trial management compliance and delivery. I have over 28 years of clinical experience as a nurse, clinical research regulatory specialist, study coordinator, and clinical trial manager in the pharmaceutical industry. My years of Clinical Research experience include Clinical Research Coordination within high volume site, Global Clinical Trial Management within large pharmaceutical companies & CRO’s, auditing procedures of the Trial Master Files (TMF) for inspection readiness as a TMF Lead, Sponsored Trials, and Project Management for People and Business Groups. My skillset includes working directly with global cross functional team leaders in pre-clinical bid defense, SAL, SSU, Data Management, global clinical supply including import/export tasks, medical management, and IRT vendors to conduct and deliver high quality studies. I have vast experience managing direct reports with a proven track record in successful line management, training & mentoring, and Subject Matter Expert Teams working to develop Sponsor integration with TransCelerate. My therapeutic indication experience includes Cardiovascular (Device, IND, and Post Market), Oncology (Hematology), Infectious Disease, NASH, Women’s Health, and Dermatology, Phases I-IV. My Clinical Trial Management experience has afforded me the ability to oversee clinical portions of study budgets, developing study plans, train Clinical Research Associates, review CRA MV reports, execute successful subject enrollment and retention activities, mindfulness to identify and mitigate risks that may impact clinical delivery by implementing corrective action plans, as well as liaise with Sponsors and vendors providing study metrics on all clinical activities. My career has brought me full circle in the clinical research industry, allowing me to fully understand the dynamics and life cycle of study execution from the site perspective, Sponsor protocol management perspective, as well as working within the CRO industry to work on bid defenses to acquire new studies, while also maintaining important client relationships for ongoing studies.

Julia AlJumaily

I am a skilled and experienced clinical research professional with a proven record of accomplishment...
5121 Chilkoot Street, Tampa, United States

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Julia AlJumaily’s Email jaljumaily@iconplc.com

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Julia AlJumaily’s Location 5121 Chilkoot Street, Tampa, United States

Julia AlJumaily’s Current Industry Icon

Julia AlJumaily’s Prior Industry Syneos Health | Romark | Bristol Myers Squibb | Bay Area Cardiology | Brandon Regional Hospital

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Work Experience

Icon

Clinical Trial Manager

2021-04-01 00:00:00 - Present

Syneos Health

Global TMF Operations Lead at Syneos Health

2019-11-01 00:00:00 - 2021-02-01 00:00:00

Romark

Clinical Trial Support Manager

2019-02-01 00:00:00 - 2019-09-01 00:00:00

Bristol Myers Squibb

Clinical Trials Associate

2016-09-01 00:00:00 - 2019-01-01 00:00:00

Bay Area Cardiology

Lead Clinical Research Nurse / Regulatory Specialist

1999-02-01 00:00:00 - 2016-09-01 00:00:00

Brandon Regional Hospital

LPN

1996-08-01 00:00:00 - 2000-07-01 00:00:00

Skills

No Skills Available

Languages

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FAQ About Julia AlJumaily

Julia AlJumaily is located at
5121 Chilkoot Street, Tampa, United States

Julia AlJumaily is a I am a skilled and experienced clinical research professional with a proven record of accomplishments ensuring trial management compliance and delivery. I have over 28 years of clinical experience as a nurse, clinical research regulatory specialist, study coordinator, and clinical trial manager in the pharmaceutical industry. My years of Clinical Research experience include Clinical Research Coordination within high volume site, Global Clinical Trial Management within large pharmaceutical companies & CRO’s, auditing procedures of the Trial Master Files (TMF) for inspection readiness as a TMF Lead, Sponsored Trials, and Project Management for People and Business Groups. My skillset includes working directly with global cross functional team leaders in pre-clinical bid defense, SAL, SSU, Data Management, global clinical supply including import/export tasks, medical management, and IRT vendors to conduct and deliver high quality studies. I have vast experience managing direct reports with a proven track record in successful line management, training & mentoring, and Subject Matter Expert Teams working to develop Sponsor integration with TransCelerate. My therapeutic indication experience includes Cardiovascular (Device, IND, and Post Market), Oncology (Hematology), Infectious Disease, NASH, Women’s Health, and Dermatology, Phases I-IV. My Clinical Trial Management experience has afforded me the ability to oversee clinical portions of study budgets, developing study plans, train Clinical Research Associates, review CRA MV reports, execute successful subject enrollment and retention activities, mindfulness to identify and mitigate risks that may impact clinical delivery by implementing corrective action plans, as well as liaise with Sponsors and vendors providing study metrics on all clinical activities. My career has brought me full circle in the clinical research industry, allowing me to fully understand the dynamics and life cycle of study execution from the site perspective, Sponsor protocol management perspective, as well as working within the CRO industry to work on bid defenses to acquire new studies, while also maintaining important client relationships for ongoing studies.

Julia AlJumaily currently works in the Icon |

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Julia AlJumaily has prior
experience in the following industries:
Syneos Health | Romark | Bristol Myers Squibb | Bay Area Cardiology | Brandon Regional Hospital

Julia AlJumaily has the following professional experience:
Icon | Syneos Health | Romark | Bristol Myers Squibb | Bay Area Cardiology | Brandon Regional Hospital