Top 40 Clinical research coordinator Jobs in Asheville Nc

FSP - Assistant Clinical Research Associate (ACRA)
Thermo Fisher Scientific —North Carolina
- Full-time
- Remote
- Nursing
- RN License
- Customer service
11h
Experienced Clinical Research Associate - Sponsor Dedicated
Syneos - Clinical and Corporate - Prod —North Carolina
- Full-time
- Mid-level
- Bachelor's degree
- Travel
- Employee stock purchase plan
- Health insurance
Clinical Research Coordinator
Mission Health —Asheville, NC
- Full-time
- Mid-level
- Experience equivalent to degree accepted
- 1 year
- Employee stock purchase plan
- Disability insurance
Quick Apply
Family Medicine - Clinical Research Investigator
ECN Operating LLC —Asheville, NC
- Part-time
- Mid-level
- Geriatrics
- Communication skills
Quick Apply
PTA - Coordinator of Clinical Education - Faculty/Instructor
SOUTH COLLEGE —Asheville, NC
- Full-time
- Classroom
- Physical & Rehabilitation Medicine
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
4d
Clinical Coordinator Sleep Services
Mission Hospital —Asheville, NC
- Part-time
- Mid-level
- Children
- 1 year
- Employee stock purchase plan
- Disability insurance
Quick Apply
Med Surg Clinical Nurse Coordinator
Mission Hospital —Asheville, NC
- Full-time
- Surgery
- Mid-level
- Children
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Nurse Coordinator Med-Surg Neuro
Mission Hospital —Asheville, NC
- Part-time
- Mid-level
- Children
- Neurology
- Employee stock purchase plan
- Disability insurance
Quick Apply
Renal Med Surg Clinical Nurse Coordinator
Mission Hospital —Asheville, NC
- Full-time
- Bachelor of Science
- Mid-level
- Children
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Nurse Coordinator Pulmonary Med Surg
Mission Hospital —Asheville, NC
- Full-time
- Mid-level
- Children
- Medical-Surgical
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Nurse Coordinator General Surgery
Mission Hospital —Asheville, NC
- Full-time
- Surgery
- Mid-level
- Children
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Nurse Coordinator Medical Cardiology SD
Mission Hospital —Asheville, NC
- Full-time
- Mid-level
- Children
- Experience equivalent to degree accepted
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Nurse Coordinator PCU
Mission Hospital —Asheville, NC
- Full-time
- Mid-level
- Children
- 1 year
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Nurse Coordinator Inpatient Rehab
CarePartners —Asheville, NC
- Full-time
- Mid-level
- Home Health
- 1 year
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Nurse Coordinator Emergency Room
Mission Hospital —Asheville, NC
- Full-time
- Mid-level
- Children
- Pediatrics
- Employee stock purchase plan
- Disability insurance
Quick Apply
9d
Clinical Nurse Coordinator - FT - Days - Rehab
CarePartners —Asheville, NC
- Full-time
- Mid-level
- Home Health
- 1 year
- Employee stock purchase plan
- Disability insurance
Quick Apply
9d
Clinical Nurse Coordinator CICU
Mission Hospital —Asheville, NC
- Full-time
- Mid-level
- Children
- 1 year
- Employee stock purchase plan
- Disability insurance
Quick Apply
8d
Clinical Nurse Coordinator OR
Mission Hospital —Asheville, NC
- Full-time
- Surgery
- Mid-level
- Children
- Employee stock purchase plan
- Disability insurance
Quick Apply
Tele Med Surg Clinical Nurse Coordinator
Mission Hospital —Asheville, NC
- Full-time
- Bachelor of Science
- Mid-level
- Children
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Nurse Coordinator Med-Surg Neuro
Mission Hospital —Asheville, NC
- Full-time
- Mid-level
- Children
- Neurology
- Employee stock purchase plan
- Disability insurance
Quick Apply

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FSP - Assistant Clinical Research Associate (ACRA)

Thermo Fisher Scientific -
North Carolina

Apply Now

Job Details

Full-time
11 hours ago

Qualifications

Nursing
Document review (document control)
RN License
Customer service
English
Invoice payment processing
ICH guidelines
Expense reports
Bachelor's degree
Clinical information systems
Vendor communication
Clinical trial standard operating procedures
Productivity software
Data collection
Root cause analysis
Clinical research documentation
Grammar Experience
Standard operating procedures (SOPs)
Medical terminology
Documentation review
Communication skills
Technical Proficiency
Entry level
Time management

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to perform remote activities on assigned projects in liaison with the CRA and study Clinical Lead. As an Assistant Clinical Research Associate, you'll provide support with site preparedness, logistical support to the monitoring process, and assist with assigned tasks for site management and remote monitoring in accordance with SOPs and regulatory guidelines. You may be assigned limited site contact activities during study start-up, site management, recruitment, and close-out phases.

What You’ll Do:

Completes study and site management activities as defined in task matrix, andas applicable and directed for study assigned.
Completes and documents study-specific training.
Orients and trains on any study-specific systems.
Provides in-house support during pre-study assessments and with pre-study assessment waivers, as agreed for project.
Supports to customize Site ICF with site contact details, as needed.
Performs remote review of EMR/EHR checklist and supports collection, as applicable assessments.
Verifies document collection and RCR submission status; updates site EDL and verifies site information.
Reviews patient facing materials and review translations, as directed.
Supports site staff with the vendor related qualification process, where applicable.
Provides support by ensuring system access is requested/granted and revoked for relevant site staff during pre-activation and subsequent course of the study.
Provides support to follow-up on site staff training, as applicable.
Coordinates and supports logistics for IM attendance, as directed.
Supports maintenance of vendor trackers, as directed.
Coordinates study/site supply management during pre-activation and subsequentcourse of the study.
Supports Essential Document collection, review and updating in systems, as applicable.
Follows up and supports on missing study vendor data like ECGs, lab samples, and e-diaries, as directed.
Supports ongoing remote review of centralized monitoring tools, as directed.
Supports Site payments processes by coordinating with various functional departments within organization and site. Supports system updates and reconciliations, as directed and follows-up on site invoices throughout the study period.
Performs reconciliation tasks on assigned trials including but not limited to CRF and query status, deviations, SAEs and safety reports, as applicable.
Verifies document collection status in company systems and drives action for missing/incomplete/expired documents and open document findings, as directed.
May perform other assigned site management tasks, as directed by CRA and as per Task Matrix.
May perform a specific role profile for FSP opportunities according to Client requests.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.

Education and Experience Requirements:

Bachelor's degree in a life science discipline or related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Basic medical/therapeutic area knowledge and understanding of medical terminology
Ability to attain and maintain a working knowledge of ICH GCP, applicable regulations and company procedural documents
Effective oral and written communication skills
Excellent interpersonal and customer service skills
Good organizational and time management skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively
Proven flexibility and adaptability
Ability to work in a team or independently, as required
Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
Proficient computer skills with good knowledge of MS Office ability to learn and use appropriate software. Leverage modern technology when applicable
Ability to extract pertinent information from all study documents, electronic study data systems, CTMS and dashboards
Excellent English language and grammar skills

Working Conditions and Environment:

Work is performed most of the time in an office or home office environment.; occasional travel toclinics/hospitals may be required.
Exposure to electrical office equipment.
The Assistant CRA role does not involve regular travel, however, any direct, promotional opportunities in the CRA career track will require frequent travel (60-80%).

Apply Now

Refine Your Search

clinical research coordinator jobs in asheville nc

FSP - Assistant Clinical Research Associate (ACRA)

Experienced Clinical Research Associate - Sponsor Dedicated

Clinical Research Coordinator

Family Medicine - Clinical Research Investigator

PTA - Coordinator of Clinical Education - Faculty/Instructor

Clinical Coordinator Sleep Services

Med Surg Clinical Nurse Coordinator

Clinical Nurse Coordinator Med-Surg Neuro

Renal Med Surg Clinical Nurse Coordinator

Clinical Nurse Coordinator Pulmonary Med Surg

Clinical Nurse Coordinator General Surgery

Clinical Nurse Coordinator Medical Cardiology SD

Clinical Nurse Coordinator PCU

Clinical Nurse Coordinator Inpatient Rehab

Clinical Nurse Coordinator Emergency Room

Clinical Nurse Coordinator - FT - Days - Rehab

Clinical Nurse Coordinator CICU

Clinical Nurse Coordinator OR

Tele Med Surg Clinical Nurse Coordinator

Clinical Nurse Coordinator Med-Surg Neuro

I want to receive the latest job alert for clinical research coordinator in asheville nc

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