Top 148 Of science Jobs in Idaho

Sr CRA (Level I) - FSP - Oncology (Central/West Coast)
Thermo Fisher Scientific —Idaho
- Full-time
- RN License
- Computer literacy
- Writing skills
6d
Environmental Scientist
Omega Technical Services —Idaho Falls, ID
- $150,000 - $190,000 a year
- Full-time
- 5 years
- Mid-level
- Bachelor's degree
- AD&D insurance
- Paid holidays
12d
Chemical Coordinator, Intermediate
Naval Nuclear Laboratory —Idaho Falls, ID
- $70,900 - $108,500 a year
- Pass drug screening
- Mid-level
- High school diploma or GED
- Wellness program
- Paid parental leave
Fisheries Biologist
State of Idaho —Idaho
- $28.94 - $36.17 an hour
- Full-time
- Doctoral degree
- Ability to walk for extended periods
- Public speaking
- Paid parental leave
- Paid holidays
Clinical Research Coordinator
Paradigm Clinical Research Center —Boise, ID
- $55,000 - $65,000 a year
- Full-time
- Background check
- Mid-level
- Master's degree
- Health insurance
- Dental insurance
Quick Apply
Principal Data Scientist - AI Trainer
DataAnnotation —Boise, ID
- $50 - $100 an hour
- Part-time
- Remote
- Computer Science
- Writing skills
- English
- Flexible schedule
Quick Apply
13d
Clinic Research Coordinator - MA
IDAHO GASTROENTEROLOGY ASSOCIATES, LLP —Meridian, ID
- Full-time
- Bilingual
- BLS Certification
- Mid-level
- Paid jury duty
- Paid holidays
14d
Senior Data Scientist - AI Trainer
DataAnnotation —Idaho
- $50 - $100 an hour
- Part-time
- Remote
- Computer Science
- English
- 3 years
- Flexible schedule
Quick Apply
Laboratory Technician- Day Shift
Darigold, Inc. —Caldwell, ID
- Day shift
- Background check
- Pass drug screening
- Mid-level
- Paid parental leave
- Paid holidays
Quick Apply
Lab Technologist, Skaggs Treasure Valley Anatomy & Physiology Laboratories (1804)
Idaho State University —Meridian, ID
- $65,000 - $69,000 a year
- 6 years
- Laboratory experience
- Mid-level
- Health insurance
- Dental insurance
8d
Clinical Project Manager - Oncology (Client Dedicated/Remote)
サイネオス・ヘルス —Idaho
- $120,000 - $135,000 a year
- Remote
- Mid-level
- 3 years
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Science & Medicine Advisor
American Heart Association —Boise, ID
- $110,000 - $120,000 a year
- Full-time
- Medicine
- Office
- Doctor of Philosophy
- Wellness program
- Paid holidays
8d
Clinical Scientist - Cardiovascular
サイネオス・ヘルス —Idaho
- Remote
- Mid-level
- Cardiology
- Employee stock purchase plan
- Health insurance
Clinical Scientist - Oncology
サイネオス・ヘルス —Idaho
- Remote
- Mid-level
- Employee stock purchase plan
- Health insurance
Research Assistant
Clinical Research Prime —Idaho Falls, ID
- Medical office experience
- Clinic
- Communication skills
Clinical Scientist - Ophthalmology
サイネオス・ヘルス —Idaho
- Remote
- Mid-level
- Employee stock purchase plan
- Health insurance
Medical Lab Scientist NonCert
St. Luke's Health System —Mountain Home, ID
- Full-time
- Bachelor's degree
- Mentoring
- Entry level
Quick Apply
Medical Lab Scientist
St. Luke's Health System —Twin Falls, ID
- Part-time
- Bachelor's degree
- Entry level
- Under 1 year
Quick Apply
12d
Technician, Lab (Thompson Creek)
Centerra Gold Inc —Clayton, ID
- $32.78 - $43.71 an hour
- High school diploma or GED
- Communication skills
- Entry level
- Disability insurance
- Dental insurance
8d
Data Scientist
Micron —Boise, ID
- Computer Science
- Mid-level
- Master's degree
- Employee stock purchase plan
- Paid holidays

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Sr CRA (Level I) - FSP - Oncology (Central/West Coast)

Thermo Fisher Scientific -
Idaho

Apply Now

Job Details

Full-time
6 days ago

Qualifications

Customer communication
Driver's License

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior Clinical Research Associate (Level I) – 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 and coordinate all aspects of the clinical monitoring and site management process. As a Senior Clinical Research Associate (Level I), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You’ll Do:

Monitors investigator sites with a risk-based monitoring approach: applies rootcause analysis (RCA), critical thinking and problem-solving skills to identify siteprocesses failure and corrective/preventive actions to bring the site intocompliance and decrease risks. Ensures data accuracy through SDR, SDV andCRF review as applicable through on-site and remote monitoring activities.Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required.
Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.
Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).
Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:

Bachelor's degree in a life sciences 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 2+ years as a clinical research monitor).
Valid driver's license where applicable
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:

Effective clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
Ability to manages Risk Based Monitoring concepts and processes
Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
Ability to maintain customer focus through the utilization of good listening skills, attention to detailand the ability to perceive customers’ underlying issues
Effective interpersonal skills
Strong attention to detail
Effective organizational and time management skills
Ability to remain flexible and adaptable in a wide range of scenarios
Ability to work in a team or independently as required
Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software
Good English language and grammar skills
Good presentation skills

Working Conditions and Environment:

Working Conditions and Environment:
Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals.
May also include extended overnight stays.
Exposure to biological fluids with potential exposure to infectious organisms.
Personal protective equipment required such as protective eyewear, garments and gloves.
Exposure to fluctuating and/or extreme temperatures on rare occasions.
Must be able to comply with specific sponsor/client/site requirements, even if not required by Thermo Fisher Scientific (e.g., disclosure of vaccination status, or other personal information). On some occasions, this information may be required to be provided directly to sponsor/client/site.

Apply Now

Refine Your Search

of science jobs in idaho

Sr CRA (Level I) - FSP - Oncology (Central/West Coast)

Environmental Scientist

Chemical Coordinator, Intermediate

Fisheries Biologist

Clinical Research Coordinator

Principal Data Scientist - AI Trainer

Clinic Research Coordinator - MA

Senior Data Scientist - AI Trainer

Laboratory Technician- Day Shift

Lab Technologist, Skaggs Treasure Valley Anatomy & Physiology Laboratories (1804)

Clinical Project Manager - Oncology (Client Dedicated/Remote)

Science & Medicine Advisor

Clinical Scientist - Cardiovascular

Clinical Scientist - Oncology

Research Assistant

Clinical Scientist - Ophthalmology

Medical Lab Scientist NonCert

Medical Lab Scientist

Technician, Lab (Thompson Creek)

Data Scientist

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