Top 7385 Clinical specialist Jobs

Clinical Research Specialist
Kelly Services —Irvine, CA
- $92,000 a year
- Full-time
- Nursing
- Bachelor of Science
- English
- Paid holidays
- Disability insurance
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Junior Clinical Trials Data Specialist
Tempus —Remote
- $46,000 - $50,000 a year
- Full-time
- Master's degree
- Bachelor's degree
- Radiology
- Health insurance
Claims Clinical Specialist
Genworth —Remote
- $86,100 - $129,000 a year
- Full-time
- Remote
- RN License
- Word processing
- Physical & Rehabilitation Medicine
- Paid holidays
- Loan repayment program
Outpatient Clinical Documentation Specialist
Boston Medical Center —Remote
- $27.88 - $40.38 an hour
- Full-time
- Remote
- Nursing
- 5 years
- Computer literacy
- Health insurance
- Dental insurance
Clinical Data Specialist
ECN Operating LLC —Remote
- $50,000 - $60,000 a year
- Full-time
- Remote
- Mid-level
- 3 years
- Travel
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Clinical Document Integrity Specialist - Part Time - Remote
Duke Health —Mooresville, NC
- 8 hour shift
- Remote
- Nursing
- Doctoral degree
- RN License
- Relocation assistance
Clinical Research Regulatory Specialist
Vitra Clinical Research —Remote
- $20 - $25 an hour
- Part-time
- HIPAA
- Mid-level
- Organizational skills
- Health insurance
- Dental insurance
Quick Apply
1d
Clinical Documentation Specialist
Johns Hopkins Health System —Baltimore, MD
- Full-time
- Nursing
- RN License
- Mid-level
- Health insurance
- Opportunities for advancement
10d
Clinical Documentation Specialist - DRG Appeals
Catholic Health —Melville, NY
- $130,000 - $170,000 a year
- Remote
- Nursing
- Microsoft Excel
- Bachelor of Science
- Health insurance
- Tuition reimbursement
Clinical Informatics Specialist
Penn Medicine —Philadelphia, PA
- Monday to Friday
- Master's degree
- Bachelor's degree
- Organizational skills
- Tuition reimbursement
Quick Apply
Clinical Documentation Specialist
Montefiore St. Luke's Cornwall —Newburgh, NY
- $90,000 - $105,000 a year
- Full-time
- Remote
- Nursing
- RN License
- English
Clinical Documentation Integrity Specialist (CDI)
Legacy Health LLC —Remote
- Full-time
- Nursing
- Acute care experience
- 1 year
- Health savings account
- Health insurance
Quick Apply
Clinical Documentation Specialist (CDI)
Solventum —Remote
- $96,000 - $132,000 a year
- Full-time
- Nursing
- Microsoft Excel
- RN License
- Health savings account
- Disability insurance
Clinical Specialist
ZERO TO THREE —Remote
- $110,000 - $120,000 a year
- Weekends as needed
- Data analysis skills
- Mid-level
- Office
- Health insurance
- Dental insurance
Clinical Specialist
VivaQuant, Inc. —Remote
- $80,000 - $90,000 a year
- Full-time
- Remote
- Nursing
- English
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Clinical Operations Specialist
SmarterDx —Remote
- $100,000 - $125,000 a year
- Remote
- Nursing
- Anatomy knowledge
- Writing skills
- Paid parental leave
- Health insurance
Clinical Informatics Specialist
Ascension —Wichita, KS
- $87,463.20 - $121,918.37 a year
- Full-time
- Mid-level
- High school diploma or GED
- Associate's degree
- Disability insurance
- Health insurance
6d
RN Clinical Consultant
Guardian Life Insurance Company —Remote
- $68,970 - $113,310 a year
- Email
- Remote
- Nursing
- Microsoft Excel
- RN License
- Disability insurance
Clinical Documentation Specialist
Managed Resources, Inc (MRI) —Remote
- $32 - $45 an hour
- Full-time
- Remote
- Medicine
- Anatomy knowledge
- RN License
- Paid holidays
- Health insurance
Clinical Documentation Specialist
Unity Hospital of Rochester —Rochester, NY
- $78,000 - $96,200 a year
- 8 hour shift
- Remote
- Nursing
- Medicine
- RN License
Quick Apply

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Clinical Research Specialist

Kelly Services -
Irvine, CA

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Job Details

Full-time
$92,000 a year

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Vision insurance
Retirement plan
Paid sick time

Qualifications

Content creation for technical audiences
Regulatory compliance
English
Technical writing experience within technology
Legal compliance
Standard operating procedures (SOPs)
Stakeholder management

Full Job Description

Clinical Research Specialist
Hybrid - onsite every Monday, Wednesday, and every other Friday
Pay Rate: 92,000

Clinical Research Specialist Requisition

Job Overview

This Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization.

Duties & Responsibilities

Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate procedures and guidelines, this position:

Serves as a Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, under supervision;
Participates in the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures;
May serve as the primary contact for clinical trial sites (e.g. site management);
Assists in the development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports);
Supports applicable trial registration (e.g. www.clinicaltrials.gov) from study initiation through posting of results and support publications as needed;
Coordinates and executes ordering, tracking, and accountability of investigational devices and trial materials;
Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel;
Interfaces and collaborates with Clinical Research Associates (CRAs);
Assists in overseeing and supports the development and execution of Investigator agreements and trial payments;
Assists in clinical data review to prepare data for statistical analyses and publications;
May perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need;
May provide on-site procedural protocol compliance and data collection support to the clinical trial sites;
Assists in tracking assigned project budgets;
May perform other duties assigned as needed;
Is responsible for communicating business related issues or opportunities to next management level. Function as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders;
Is responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures;
Should develop a strong understanding of the pipeline, product portfolio and business needs;
Generally manages work with supervision. Independent decision-making for simple situations but requires guidance for complex situations.

Experience and Education

Education

Minimum of a Bachelor’s Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.

Experience

BS with at least 2 years, MS and PhD with at least 1 year of relevant experience preferred.
Previous experience in clinical research or equivalent is desired.
Relevant industry certifications preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR, MEDDEV,…).
Clinical/medical background is a plus.
Medical device experience is a plus.

Required Knowledge, Skills, Abilities, Certifications/Licenses and Affiliations

Functional and Technical Competencies:

Good understanding of clinical research science and processes, clinical trends, and global clinical trial regulations;
Proven track record in supporting clinical projects within clinical/ surgical research setting, on time, and in compliance to SOPs and regulations;
Presentation and technical writing skills;
Written and oral English communication skills.

Leadership Competencies:

Leadership required in alignment with Company Leadership Imperatives:

Connect - Develop collaborative relationships with key internal and external stakeholders.
Shape - Actively participate in departmental process improvement activities.
Lead - Take ownership in critical scientific thinking and development of self and engage in transparent and constructive conversations.
Deliver - Strive to ensure all deliverables on allocated studies are met on time, within budget and in compliance to SOPs and regulations.

Location & Travel Requirements
Primary location for this position is Irvine, CA. At management discretion, the position may be performed remotely.
Ability to travel approximately 20% depending on the phase of the program.

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following benefits reflect Kelly's general offerings. Eligibility may vary by assignment, location, and job type. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.

Quick Apply

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Clinical Research Specialist Requisition

Job Overview

Duties & Responsibilities

Experience and Education

Education

Experience

Required Knowledge, Skills, Abilities, Certifications/Licenses and Affiliations

Functional and Technical Competencies:

Leadership Competencies:

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