Top 40 Research Jobs in Clemson Sc

Clinical Research Coordinator I
Velocity Clinical Research, Inc. —Anderson, SC
- English
- Mid-level
- Ability to sit for extended periods
- Paid holidays
- Health insurance
Quick Apply
8h
R&D Specialist
Smurfit Westrock —Anderson, SC
- $44,250 - $73,750 a year
- Full-time
- Master's degree
- Bachelor's degree
- Travel
- Health savings account
- AD&D insurance
Clinical Research Coordinator (Walhalla, SC)
SiteBridge Research, Inc. —Walhalla, SC
- $30 - $36 an hour
- Part-time
- Spanish
- English
- Mid-level
Quick Apply
Entry to Mid-Level Design Researcher
Techtronic Industries Power Equipment —Anderson, SC
- Full-time
- Marketing
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Medical Lab Tech/Scientist, Full-Time, Nights
Prisma Health —Seneca, SC
- Full-time
- Hospital
- Word processing
- No experience needed
Pharmacy Clinical Specialist
SiteLabs —Clemson, SC
- $55,000 - $70,000 a year
- Full-time
- Hybrid work
- Mid-level
- Travel
- Communication skills
- Paid holidays
- Paid time off
Quick Apply
Senior Data Scientist - AI Trainer
DataAnnotation —South Carolina
- $50 - $100 an hour
- Part-time
- Remote
- Computer Science
- English
- 3 years
- Flexible schedule
Quick Apply
Thermal R&D Engineer
Airsys Cooling Technologi —Anderson, SC
- Full-time
- Analysis skills
- Doctor of Philosophy
- Communication skills
Quick Apply
8d
R&D Product Development Engineer
Vertiv —Anderson, SC
- Engineering
- Mid-level
- Analysis skills
Postdoctoral Research Associate
Clemson University —Clemson, SC
- $68,000 a year
- Doctoral degree
- University
- Travel
- Dental insurance
- Vision insurance
Director of Research Security & Export Control
Clemson University —Clemson, SC
- Full-time
- 5 years
- University
- Bachelor's degree
Executive Director of the South Carolina Water Resources Center
Clemson University —Clemson, SC
- In person
- University
- Doctor of Philosophy
- Budgeting
13d
Postdoctoral Fellow in Neurodevelopmental Health & Education
Clemson University —Clemson, SC
- School experience
- Doctoral degree
- Residential
18h
Postdoctoral Fellow - Automotive Engineering
Clemson University —Clemson, SC
- University
- Doctor of Philosophy
- Senior level
18h
Evergreen - Post Doctoral Fellow - Mechanical Engineering
Clemson University —Clemson, SC
- University
- Doctor of Philosophy
- Senior level
Post Doctoral Fellow
Clemson University —Clemson, SC
- University
- Doctor of Philosophy
- Senior level
Post Doctoral Fellow - Environmental Engineering & Earth Sciences
Clemson University —Clemson, SC
- Online Application
- University
- Doctor of Philosophy
- Senior level
Post Doctoral Fellow - Department of Chemistry
Clemson University —Clemson, SC
- University
- Doctor of Philosophy
- Senior level
3h
Post Doctoral Fellow in Learning-based Control for Controlled Environment Agriculture (Mechanical Engineering)
Clemson University —Clemson, SC
- Full-time
- University
- Doctor of Philosophy
- Senior level
Post Doctoral Fellow - Department of Physics and Astronomy
Clemson University —Clemson, SC
- Math
- University
- Doctor of Philosophy

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Clinical Research Coordinator I

Velocity Clinical Research, Inc. -
Anderson, SC

Quick Apply

Job Details

8 hours ago

Benefits

Paid holidays
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching

Qualifications

Injectable medication administration
Phone communication
English
Phlebotomy specimen handling
Fax machines
Multi-line phone systems
Productivity software
Faxing
Medical terminology
Delegation
Client interaction via phone calls

Full Job Description

Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.

As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.

Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.

Summary:

The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.

Duties/Responsibilities:

Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.
Implement research and administrative strategies to successfully manage assigned protocols.
Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
Apply good documentation practices when collecting and correcting data, transferring data to sponsor/CRO data capture systems, and resolving queries
Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
Ensure patient safety is upheld and all adverse events, serious adverse events, and adverse events of special interest are followed and reported in accordance with the protocol and Velocity SOPs.
Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely manner
Ensure staff are delegated and trained appropriately and documented
Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.
Evaluate potential subjects for participation in clinical trials including phone and in person pre screens.
Execute recruitment strategies defined by Clinical Research Team
Understand key timelines, endpoints, required vendors, and patient population for each assigned protocol.
Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope
Promote respect for cultural diversity and conventions with all individuals.

Education/Experience:

Bachelor’s degree with 1 year of relevant experience in the life science industry OR
Associate’s degree with 2 years of relevant experience in the life science industry OR
High School Graduate and/or technical degre with minimum of 3 years relevant experience in the
life science industry

Required Licenses/Certifications:

Phlebotomy if applicable and required by state law
Intramuscular dose administration and preparation if applicable and required by state law

Required Skills:

Demonstrated knowledge of medical terminology
Demonstrated ability in the use of the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
Demonstrated bility to work in a fast-paced environment
Demonstrated verbal, written, and organizational skills
Demonstrated interpersonal and communication skills
Demonstrated ability to work as a team player
Demonstrated ability to read, write, and speak English
Demonstrated ability to multi-task
Demonstrated ability to follow written guidelines
Demonstrated ability to work independently, plan and prioritize with some guidance
Demonstrated ability to be flexible/adapt as daily schedule may change rapidly
Must be detail oriented
Demonstrated problem solving and strategic decision making ability.
Proficient ability to accept individual responsibility for actions taken and demonstrate professionalism when judged, critiqued and/or praised.

Required Physical Abilites:

Sit or stand for long periods of time
Travel locally and nationally
Communicate in person and by a telephone
Limited walking required
Limited to lifting up to 30 pounds

NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required. Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change. All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.

Quick Apply

Refine Your Search

research jobs in clemson sc

Clinical Research Coordinator I

R&D Specialist

Clinical Research Coordinator (Walhalla, SC)

Entry to Mid-Level Design Researcher

Medical Lab Tech/Scientist, Full-Time, Nights

Pharmacy Clinical Specialist

Senior Data Scientist - AI Trainer

Thermal R&D Engineer

R&D Product Development Engineer

Postdoctoral Research Associate

Director of Research Security & Export Control

Executive Director of the South Carolina Water Resources Center

Postdoctoral Fellow in Neurodevelopmental Health & Education

Postdoctoral Fellow - Automotive Engineering

Evergreen - Post Doctoral Fellow - Mechanical Engineering

Post Doctoral Fellow

Post Doctoral Fellow - Environmental Engineering & Earth Sciences

Post Doctoral Fellow - Department of Chemistry

Post Doctoral Fellow in Learning-based Control for Controlled Environment Agriculture (Mechanical Engineering)

Post Doctoral Fellow - Department of Physics and Astronomy

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