Top 74 Clinical research associate Jobs in Wisconsin

Clinical Research Associate II - US Central - Multiple Therapeutic Areas Available
Thermo Fisher Scientific —Wisconsin
- $66,800 - $120,000 a year
- Full-time
- Background check
- Nursing
- RN License
- Commuter assistance
- Paid parental leave
8d
Project Coordinator I (US Remote)
MERIT CRO, Inc. —Madison, WI
- Full-time
- Remote
- Computer Science
- Bachelor's degree
- Continuous improvement
- Paid holidays
- Disability insurance
Quick Apply
SENIOR CLINICAL RESEARCH ASSOCIATE
SPAULDING CLINICAL RESEARCH LLC —West Bend, WI
- $115 - $125 a day
- Full-time
- Remote
- Microsoft Word
- Nursing
- Microsoft Excel
Quick Apply
3d
Clinical Research Coordinator - Full Time
Mercy Health System Corporation —Janesville, WI
- $27.17 - $42.11 an hour
- Full-time
- Microsoft Excel
- Hospital
- Mid-level
- Paid parental leave
- Health savings account
Quick Apply
8d
Clinical Research Coordinator I - Emergency Medicine
The Medical College of Wisconsin, Inc. —Milwaukee, WI
- Weekends as needed
- Writing skills
- Databases
- Math
- Paid parental leave
- Paid holidays
Quick Apply
2d
Research Coordinator, Advocate Aurora Research Institute
Advocate Aurora Health —Kenosha, WI
- $30.70 - $46.05 an hour
- Full-time
- Nursing
- Patient monitoring
- Mid-level
Assistant, Clinical Research Unit
UW Health —Madison, WI
- $20.69 - $28.01 an hour
- Part-time
- Databases
- High school diploma or GED
- Organizational skills
- Paid parental leave
- Health insurance
10d
Researcher I
University of Wisconsin–Madison —Madison, WI
- $63,439 a year
- Weekends as needed
- Psychiatry
- Master's degree
- Supervising experience
9d
Research Regulatory Specialist - Wisconsin Institute of Neuroscience
The Medical College of Wisconsin, Inc. —Milwaukee, WI
- Full-time
- Microsoft Word
- Mid-level
- Office
- Paid parental leave
- Paid holidays
Quick Apply
Clinical Research Assistant III - Surgery
The Medical College of Wisconsin, Inc. —Milwaukee, WI
- Full-time
- Surgery
- English
- Mid-level
- Paid parental leave
- Paid holidays
Quick Apply
Assistant Clinical Research
Versiti, Inc. —Milwaukee, WI
- Full-time
- Microsoft Excel
- Microsoft Outlook
- High school diploma or GED
- Paid holidays
- Disability insurance
Oncology Imaging Quality Control Specialist II (US Remote)
MERIT CRO, Inc. —Madison, WI
- Full-time
- Remote
- 5 years
- Computer literacy
- Mid-level
- AD&D insurance
- Paid holidays
Quick Apply
7d
Research Nurse
University of Wisconsin–Madison —Madison, WI
- $72,500 - $90,000 a year
- Part-time
- Hybrid work
- Nursing
- RN License
- Mid-level
- Retirement plan
Clinical Research Assistant II (Child Neurology)
The Medical College of Wisconsin, Inc. —Milwaukee, WI
- Full-time
- Writing skills
- High school diploma or GED
- Clinic
- Paid parental leave
- Paid holidays
Quick Apply
Clinical Research Nurse
Children's Wisconsin —Milwaukee, WI
- Part-time
- Nursing
- Microsoft Outlook
- RN License
Clinical Research Nurse / Open to RN's, and LPN's / Madison, WI (On-Site)
Fortrea —Madison, WI
- Full-time
- Nursing
- RN License
- Clinic
- Free parking
- Disability insurance
Clinical Research Quality Assurance Specialist II - Cancer Center
The Medical College of Wisconsin, Inc. —Milwaukee, WI
- Full-time
- Writing skills
- Mid-level
- University
- Paid parental leave
- Paid holidays
Quick Apply
Clinical Research Coordinator II - Psychiatry
The Medical College of Wisconsin, Inc. —Milwaukee, WI
- Full-time
- Psychiatry
- Computer literacy
- Mid-level
- Paid parental leave
- Paid holidays
Quick Apply
9d
Clinical Research Nurse I /Madison, WI (On-Site)
Fortrea —Madison, WI
- Full-time
- CPR Certification
- Nursing
- Bachelor of Science
- Disability insurance
- Health insurance
SCREENING COORDINATOR
SPAULDING CLINICAL RESEARCH LLC —West Bend, WI
- $50,000 a year
- Full-time
- English
- Mid-level
- High school diploma or GED
Quick Apply

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Clinical Research Associate II - US Central - Multiple Therapeutic Areas Available

Thermo Fisher Scientific -
Wisconsin

Apply Now

Job Details

Full-time
$66,800 - $120,000 a year
8 days ago

Benefits

Commuter assistance
Paid parental leave
Caregiver leave
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Vision insurance
Life insurance

Qualifications

Customer communication
Clinical audit and monitoring
Driver's License

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Research Associate (Level II) – 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 five 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 Clinical Research Associate (Level II), 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.

Required Qualifications

1–2 years of traveling on-site monitoring experience.

Therapeutic experience in at least one of the following: Oncology, Ophthalmology, Neurology, Cardiology, Rare Disease, Respiratory, Obesity, and/or Pulmonary.

Candidates must live within 60 miles of the nearest major airport. Up to 80% travel is expected.

Must be legally authorized to work in the United States without sponsorship.

Must be able to pass a comprehensive background check, including a drug screening.

What You’ll Do:

Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks.

Ensures data accuracy through SDR, SDV and CRF 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.
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. Performs 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.
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).
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 the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members.
Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:

Bachelor's degree in a life sciences related fieldor 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 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship.
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:

Proven clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to: critical mindset, in-depthinvestigation for appropriate root cause analysis and problem solving
Ability to manage Risk Based Monitoring concepts and processes
Good 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 detail and the ability to perceive customers’ underlying issues
Good organizational and time management skills
Effective interpersonal skills
Attention to detail
Ability to remain flexibile and adaptable in a wide range of scenarios
Ability to work in a team or independently as required
Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
Good English language and grammar skills
Good presentation skills

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

Compensation and Benefits

The salary range estimated for this position based in Illinois is $66,800.00–$120,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Apply Now

Refine Your Search

clinical research associate jobs in wisconsin

Clinical Research Associate II - US Central - Multiple Therapeutic Areas Available

Project Coordinator I (US Remote)

SENIOR CLINICAL RESEARCH ASSOCIATE

Clinical Research Coordinator - Full Time

Clinical Research Coordinator I - Emergency Medicine

Research Coordinator, Advocate Aurora Research Institute

Assistant, Clinical Research Unit

Researcher I

Research Regulatory Specialist - Wisconsin Institute of Neuroscience

Clinical Research Assistant III - Surgery

Assistant Clinical Research

Oncology Imaging Quality Control Specialist II (US Remote)

Research Nurse

Clinical Research Assistant II (Child Neurology)

Clinical Research Nurse

Clinical Research Nurse / Open to RN's, and LPN's / Madison, WI (On-Site)

Clinical Research Quality Assurance Specialist II - Cancer Center

Clinical Research Coordinator II - Psychiatry

Clinical Research Nurse I /Madison, WI (On-Site)

SCREENING COORDINATOR

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