Clinical Trials Data Specialist Jobs

Minimum 3 years of document management experience.

5+ years of document management experience

Experience working with clinical electronic databases, preferably Medidata Rave

Experience in organizing documents for internal and external audits

Facilitate the design and development of data collection forms, instructions and procedures.

Develop and maintain flow diagrams developed to document coding processes around eligibility and randomization.

At Least 3 years of experience in clinical data management and computer savvy. Some project management skills are needed.

Clinical data management experience needed.

They must be open to do menial tasks if they have 5 years experience.

Hybrid role (4 days onsite and 1 day remote)

A team player and flexible; quick and eager to enter into ADC.

Product: a sensor that will b put on the patient

Bachelor's degree or graduate degree and at least 4 years of experience in a quantitative or computational function

4 years of experience in R, Python, or SQL.

Experience in designing and executing robust and reproducible statistical analyses in the context of epidemiology and observational research with healthcare data

Experience processing large data from various data sources

Experience handling protected patient health information

Knowledge of at least one of the following: Tableau, Power Bi, Alteryx, Spotfire, or other BI intelligence tools

High School education or equivalent

Assists study staff with any concerns or questions by promptly providing the information and feedback as requested

Enters data in databases, generates reports, performs data/database maintenance, performs data tracking, and performs queries.

Provides auditable trail of documentation with consistency among data base, records and required reports

Provides reports on grant progress and assists in troubleshooting

Serves as liaison for Research Institute with all departments involved with the study.

Desired Experience, Skills and Abilities:

Enter country level information in BI Clinical Trial Management System (CTMS) and related systems.

Under the direction of the CTL/CTM or Feasibility Manager (depending on the task/activity), the CTO will:

Create trial specific slide decks, training material, etc. in accordance with BI requirements.

Excellent communication skills (written and oral)

In addition to the CTO responsibilities and duties, they may provide assistance in leading the trial team:

Needs to be communicative and responsive and know when to escalate and communicate issues to management.

Oncology clinical research experience is required.

Any experience working with solid tumors is a big plus.

Demonstrated computer skills with Microsoft Office applications.

Vitalief is offering a $3,500 sign-on bonus for this position!

You'll impact clinical research in various therapeutic areas, including oncology, and improve outcomes for diverse populations.

Manage and effectively communicate Firm’s travel needs to vendors/resources.

Work on developing internal processes to enhance travel experience for attorneys and staff.

A minimum of 5 years of experience in travel or hotel sales and a Bachelor’s Degree.

Establishment and promotion of strong working relationships with external contacts and suppliers to ensure the Firm’s needs are understood and met.

Creation and dissemination of travel resource communication to the Firm.

Develop relationships with paralegals to assist with their trial related travel needs including contracting hotel guest room and meeting space.

Knowledge, Skills And Abilities (required)

Experience with Electronic Data Capture (EDC)

Some knowledge of medical terminology

Strong clerical, interpersonal, and organizational skills.

Ability to exercise judgment and employ basic reasoning skills.

Extraction and entry of required clinical data from medical records and patient research charts/reports to Clinical Research Forms (eCRFs/CRFs).