Top 22477 Database Research Jobs

Clinical Research Associate II
SystImmune —Remote
- $80,000 - $110,000 a year
- Full-time
- Remote
- Microsoft Excel
- Mid-level
- Bachelor's degree
Sr. Clinical Research Associate
SystImmune —Remote
- $90,000 - $130,000 a year
- Full-time
- Remote
- Microsoft Excel
- Mid-level
- Bachelor's degree
- Paid holidays
- Disability insurance
Residential Salesperson: Full-Time
Patco Construction Inc —Sanford, ME
- Full-time
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- Residential
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SafeHouse Ministries —Columbus, GA
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- Public speaking
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Probate/Trust Administration Paralegal
GIANELLI, FRIEDMAN, JEFFRIES & McKERNAN —Modesto, CA
- $62,400 - $83,200 a year
- Extended hours
- Microsoft Word
- Background check
- Microsoft Outlook
- Health insurance
- Dental insurance
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Grants Administrator
YWCA Missoula —Missoula, MT
- $70,000 - $75,000 a year
- Weekends as needed
- Background check
- Management
- 5 years
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Assistant Real Property Lister and Real Estate/Vital Records Clerk
Ashland County —Ashland, WI
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- Full-time
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- 1 year
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- Dental insurance
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11d
Medical Director - Outpatient Opioid Treatment Program
Reflections of Hope —Wilmington, NC
- Part-time
- Acute care
- Background check
- Medicine
- Health insurance
- Dental insurance
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Business Government Contracting Counselor
Oregon Native American Chamber —Portland, OR
- $32 - $38 an hour
- Weekends as needed
- Hybrid work
- Public speaking
- Mid-level
- Business development experience
- 401(k)
- Paid time off
Quick Apply
13d
City Attorney
City of Nixa —Nixa, MO
- $149,090 - $162,508 a year
- Full-time
- Background check
- Management
- Word processing
- Health savings account
- Health insurance
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Registrar
Newport Restoration Foundation —Newport, RI
- $60,000 - $65,000 a year
- Full-time
- Mid-level
- 3 years
- Master's degree
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RN for Clinical Research Recruiting
SEC Clinical Research —Andalusia, AL
- $28 - $34 an hour
- Full-time
- RN License
- HIPAA
- Mid-level
- Health insurance
- Dental insurance
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4d
Automotive Service Writer
TEAM Chevy Manistique —Manistique, MI
- $18 - $25 an hour
- Full-time
- Clean driving record
- Writing skills
- Research
- Health insurance
- Dental insurance
Quick Apply
Estimator Heavy Civil
Thalle Construction Company —Alvarado, TX
- Weekends as needed
- Construction site
- Bachelor of Science
- Research
- Paid holidays
- Disability insurance
Quick Apply
Marketing & Donor Database Specialist (Salesforce Experience a Must!)
Catholic Charities —Seminole, FL
- $20 an hour
- Weekends as needed
- Microsoft Word
- Background check
- Computer literacy
- AD&D insurance
- Paid holidays
Quick Apply
Litigation Paralegal
Cory Watson —Memphis, TN
- $25 - $30 an hour
- 8 hour shift
- Background check
- 5 years
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Briggs Electric —Carson City, NV
- $125,000 - $150,000 a year
- Full-time
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- Ability to walk for extended periods
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Clinical Pharm Specialist –Hema/Onc and Gen Inf SCH
Catholic Health System —Buffalo, NY
- $133,731 - $200,577 a year
- Weekends as needed
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Patient Service Representative
(SDX) Scientia Diagnostics LLC —Lanoka Harbor, NJ
- $18 - $21 an hour
- Overtime
- Bilingual
- Clean driving record
- Microsoft Outlook
Quick Apply
Director, Quality & Patient Safety
Boston Medical Center —Boston, MA
- $122,000 - $177,000 a year
- Full-time
- Background check
- Nursing
- Microsoft Excel
- Health insurance
- Dental insurance
Quick Apply

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Clinical Research Associate II

SystImmune -
Remote

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Job Details

Full-time
$80,000 - $110,000 a year

Qualifications

Pharmaceutical regulatory compliance
ICH guidelines
Bachelor's degree
SharePoint
Productivity software
Clinical quality assurance standards
Oncology

Full Job Description

Remote

Full Time

Experienced

SystImmune is seeking a high quality, ambitious and experienced Clinical Research Associate II (CRA II) to support SystImmune’s clinical trials. The CRA II is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs. The CRA II must be self-motivated, independent, and able to work in a small team environment. The successful candidate will be a highly organized individual who can also multitask and adjust direction based on changing project/corporate priorities.

Job Responsibilities:

Perform Site Evaluation Visits, Site Initiation Visits, Interim monitoring visits and Close Out Visits
Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites
Responsible for ensuring investigator sites have met all contractual and regulatory requirements for site initiation and first release of study drug
Assist in the development of study/program plans (i.e., Monitoring Plan, eCRF Completion Guidelines, Data Management Plan, Safety Management Plan, etc.)
Manage patient recruitment strategies, proactively identifying barriers to recruitment while proposing solutions (i.e., study-site webinars, newsletters or other potential creative solutions)
Monitor recruitment, data quality and patient safety while on site and remotely through EDC systems and direct site communication
Liaise with study site personnel to ensure timely and correct entry of data into eCRF, including the timely resolution of data queries
Maintain project files including ethics committee approvals, curricula vitae of investigators and study personnel, clinical investigators brochure, protocols, case report forms instructions, consent documents, clinical-trial material shipping orders, start-up meeting attendance documentation, letters of agreement, lab reference ranges, and all investigator and site correspondence
Identify and complete follow- up of SAEs at study sites
Assist with data listing, data coding, patient profile reviews, database lock, and site close-out activities
Ensure appropriate and timely submission of documents to the Trial Master File
Perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP.

Qualifications:

Bachelor’s degree in health science or related field.
2+ years monitoring Oncology trials independently conducting on-site and remote monitoring visits.
Excellent verbal and written communication skills required.
Excellent organizational, multi-tasking and time management skills required.
Demonstrated experience developing/maintaining site relationships and securing compliance
Working knowledge of International Conference on Harmonization Good Clinical Practice guidelines
Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF)
Ability to travel as required (50-75%)

Compensation and Benefits:

The expected base salary range for this position is $80,000 - $110,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.

Apply Now

Refine Your Search

Database Research jobs

Clinical Research Associate II

Sr. Clinical Research Associate

Residential Salesperson: Full-Time

Director of Development

Probate/Trust Administration Paralegal

Grants Administrator

Assistant Real Property Lister and Real Estate/Vital Records Clerk

Medical Director - Outpatient Opioid Treatment Program

Business Government Contracting Counselor

City Attorney

Registrar

RN for Clinical Research Recruiting

Automotive Service Writer

Estimator Heavy Civil

Marketing & Donor Database Specialist (Salesforce Experience a Must!)

Litigation Paralegal

Project Manager

Clinical Pharm Specialist –Hema/Onc and Gen Inf SCH

Patient Service Representative

Director, Quality & Patient Safety

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