Research operations occupations Work, Jobs in Nevendon, Ess (with Salaries)

Clinical Research Assistant
Velocity Clinical Research, Inc. —Romford
- Temporary
- Computer literacy
- Writing skills
- English
4d
Clinical Research Coordinator I
Velocity Clinical Research, Inc. —Romford
- Temporary
- Computer literacy
- Writing skills
- English
3d
Community Nurse Ambassador (Flexible Ongoing Role)
CareForMe —Ilford
- £180 a day
- English
- In-person
- Communication skills
- Flexitime
Quick apply
Head of Impact & Insights
Fairtrade Foundation —London
- £66,598 a year
- Hybrid work
- Analysis skills
- Leadership
- Analytics
8d
Head of AI Safety
Moonshot —London
- £75,000 - £90,000 a year
- Full-time
- Hybrid work
- Master's degree
- Business development
- Team management
- Annual leave
- Employee assistance programme
Quick apply
Strategic Partnerships Insight Manager
Cancer Research UK —London
- £37,000 - £42,000 a year
- Full-time
- Hybrid work
- No degree
- Communication skills
5d
Clinical Research Nurse - 12 month FTC
hVIVO Services Limited —London
- Night shift
- Microsoft Word
- Nursing
- Mentoring
Senior Project Manager - Research & Evaluation (Public Affairs)
Ipsos —London
- Business development
- Continuous improvement
- Organisational skills
- Annual leave
Doctoral Programme Manager
University of Greenwich —Medway
- £38,784 - £44,746 a year
- Call to connect
- University
3d
Clinical Research Nurse
Velocity Clinical Research, Inc. —Romford
- Temporary
- Travel
- Patient care
- Data entry
4d
Clinical Research Nurse - Bank, Full-Time
hVIVO Services Limited —London
- Night shift
- Microsoft Word
- Nursing
- Mentoring

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Clinical Research Assistant

Velocity Clinical Research, Inc. -
Romford

Apply Now

Job details

Temporary
4 days ago

Qualifications

Clinical research
Clinical record keeping
Phlebotomy
Stock ordering
Computer literacy
Writing skills
Laboratory housekeeping
Filing
English
Microsoft Office Suite
Appointment booking and call handling
Data entry
Organisational skills
Front desk
Venepuncture
Good Clinical Practice (GCP)
Stock replenishment
Patient record updating
Medical terminology
Good Clinical Practice (ICH-GCP) guidelines
Research participant recruitment coordination

Full job description

Overview:

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.

Summary:

The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities.

Responsibilities:

Duties/Responsibilities:

Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs
Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations
With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations
Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable
Track, order and maintain inventory of all laboratory and study related supplies throughout course of the clinical trial
Enter source data into the sponsor's and/or vendor’s data portal and resolve basic queries in a timely manner under the direction of the Clinical Research Coordinator
Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team
Understand good documentation practices when collecting, transferring data to sponsor/CRO data capture systems and resolving queries under the direction of the Clinical Research Coordinator
Understand the informed consent process with emphasis on ensuring initial and ongoing consent of study subjects
Understand basic elements of regulatory documentation required to initiate, maintain and close a clinical research trial
Understand and participate in patient recruiting tasks including but not limited to prescreening potential subjects for clinical research trials either via phone or in person
Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
Ability to escalate potential patient safety issues such as adverse events, serious adverse events, and adverse events of special interest to the Clinical Research Team
Cleaning, organizing, and disinfecting the patient care, lab and lab equipment areas as needed
Prepare source document charts, copy and/or file medical records and study related documents as required.
Perform front office duties as needed including but not limited to answering phones, scheduling subjects, making reminder calls and updating patient tracking systems.
Other duties as assigned

Qualifications:

Education/Experience:

High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences 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 to use the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
Understanding of verbal, written, and organizational 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 be flexible/adapt as daily schedule may change rapidly

Required Physical Abilities:

Sit or stand for long periods of time
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.

Apply Now

Refine Your Search

research operations occupations jobs in nevendon, ess

Clinical Research Assistant

Clinical Research Coordinator I

Community Nurse Ambassador (Flexible Ongoing Role)

Head of Impact & Insights

Head of AI Safety

Strategic Partnerships Insight Manager

Clinical Research Nurse - 12 month FTC

Senior Project Manager - Research & Evaluation (Public Affairs)

Doctoral Programme Manager

Clinical Research Nurse

Clinical Research Nurse - Bank, Full-Time

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