8 S & P SPECIALIST I Jobs in Bethesda, MD

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S & P SPECIALIST I

tech-res

Bethesda, MD | Full Time

$73k-95k (estimate)

6 Months Ago

S & P SPECIALIST I

Technical Resources International, Inc.

Bethesda, MD | Full Time

$75k-100k (estimate)

0 Months Ago

S & P SPECIALIST I

TECHNICAL RESOURCES INT'L

Bethesda, MD | Full Time

$78k-102k (estimate)

0 Months Ago

S & P ASSOCIATE I

tech-res

Bethesda, MD | Full Time

$75k-97k (estimate)

6 Months Ago

S & P ASSOCIATE I

TECHNICAL RESOURCES INT'L

Bethesda, MD | Full Time

$77k-102k (estimate)

0 Months Ago

Fulfillment Specialist I

Prepaid Wireless Wholesale LLC

Bethesda, MD | Full Time

$44k-54k (estimate)

2 Months Ago

REGULATORY SPECIALIST I

TECHNICAL RESOURCES INT'L

Bethesda, MD | Full Time

$73k-95k (estimate)

0 Months Ago

Quality Assurance Specialist I/II/III - Infectious Disease (Hybrid)

Henry M. Jackson Foundation for the Advancement of Military Medicine

Bethesda, MD | Full Time

$100k-120k (estimate)

10 Months Ago

S & P SPECIALIST I

$75k-100k (estimate)

Full Time | Business Services 0 Months Ago

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Technical Resources International, Inc. is Hiring a S & P SPECIALIST I Near Bethesda, MD

Location

Bethesda, MD 20817 US (Primary)

Category

Drug Safety

Job Type

Full-Time

Education

Master's Degree

Travel

None

Job Description

Ensures compliance with TRI Standard Operating Procedures, Food and Drug Administration and World Health Organization regulations and global regulations for the reporting of adverse events to regulatory agencies
Develops and ensures the uniform and timely processing of adverse event reports
Provides medical evaluation of adverse event reports
Performs various tasks in support of clinical research including the reporting, collecting, and sharing of results and issues around adverse event reports both for currently marketed drugs as well as those in the experimental stages of development
Maintains/updates agent-specific clinical and preclinical toxicity study summary tables for investigational agents
Performs literature searches
Performs various tasks in support of clinical research including adverse event analysis and processing, serious adverse event reconciliation.
Preparation of IND safety reports for submission to the FDA; safety document or data analysis.
Clinical trial site support; reporting, collecting, and sharing of results and issues around adverse event reports both for currently marketed drugs as well as those in the experimental stages of development.
Assists in the preparation of new drug application safety updates, investigational new drug safety reports, investigator communication, product labeling/package inserts, and other reports as necessary.
May review experimental protocols and informed consent documents; and prepare, review, and edit presentations regarding safety issues.

Job Requirements

Knowledge of GCP and ICH guidelines preferred; drug development/clinical trial experience essential.
Knowledge of safety databases and/or MedDRA coding preferred.
Experience leading clinical and cross functional teams is a plus.
Must have excellent oral, written, presentation and computer skills.
2 years of academic, pharmaceutical or biotech industry or academic experience.

We are equal opportunity/affirmative action employers, committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status, or any other protected characteristic under state or local law.