Top 1786 Clinical associate Jobs in Minnesota

Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available
Thermo Fisher Scientific —Minnesota
- $66,800 - $125,000 a year
- Full-time
- Background check
- Nursing
- RN License
- Commuter assistance
- Paid parental leave
4d
Manager, Clinical Initiatives - Remote
Optum —Eden Prairie, MN
- $91,700 - $163,700 a year
- Full-time
- Remote
- Pass drug screening
- Mid-level
- 3 years
Quick Apply
3d
Senior Clinical Research Associate - CNS/Rare Disease - Central U.S. (Remote)
Worldwide Clinical Trials —Minnesota
- $97,000 - $193,000 a year
- Full-time
- Remote
- Nursing
- 5 years
- English
Behavioral Health Outpatient Therapist Clinical Trainee
Bois Forte Reservation Tribal Government —Nett Lake, MN
- From $64,417.60 a year
- Full-time
- LMFT
- Microsoft Excel
- Computer literacy
- Health insurance
- Dental insurance
1d
Licensed Clinical Psychologist- IQ Testing
Midwest Autism & Psychological Services —Minneapolis, MN
- $110 - $125 an hour
- Choose your own hours
- Hybrid work
- Doctoral degree
- Writing skills
- Mid-level
- Professional development assistance
- Flexible schedule
Quick Apply
LPCC (Licensed Professional Clinical Counselor)
New Life Treatment Center —Woodstock, MN
- $75,000 - $95,000 a year
- Full-time
- Background check
- LMFT
- Computer literacy
- Health insurance
- Paid time off
Quick Apply
Licensed Mental Health Therapist
Headway —Minneapolis, MN
- Up to $146 an hour
- Remote
- Private practice
- LMFT
- Licensed Clinical Social Worker
Licensed Mental Health Therapist
Headway —Minnesota
- Up to $146 an hour
- Remote
- Private practice
- LMFT
- Licensed Clinical Social Worker
Treatment Supervisor, Full Time/Mental Health Professional
Prairie Community Services —Marshall, MN
- From $93,600 a year
- Online Application
- Background check
- LMFT
- Psychiatry
- Health savings account
- Disability insurance
Quick Apply
Licensed Clinical Psychologist
Nowlogy —Plymouth, MN
- From $135,000 a year
- Full-time
- Hybrid work
- Background check
- Doctoral degree
- Doctor of Philosophy
- Professional development assistance
- Flexible schedule
Quick Apply
Licensed Mental Health Therapist
Headway —Rochester, MN
- Up to $146 an hour
- Remote
- Private practice
- LMFT
- Licensed Clinical Social Worker
Licensed Mental Health Therapist
Headway —Winona, MN
- Up to $146 an hour
- Remote
- Private practice
- LMFT
- Licensed Clinical Social Worker
Licensed Clinical Assistant or Licensed Hygienist - Orthodontics
Arrowhead Orthodontics —Duluth, MN
- $28 - $33 an hour
- 8 hour shift
- Background check
- Dental office
- US work authorization
- Health savings account
- Health insurance
Quick Apply
Clinical Systems Developer Lead
Mankato Clinic —Mankato, MN
- $82,472 - $123,614 a year
- Full-time
- Hybrid work
- Computer Science
- Master's degree
- Bachelor's degree
- Profit sharing
- Wellness program
Quick Apply
Mental Health Therapist or Social Worker
Psychiatric Medical Care —Baudette, MN
- Up to $85,000 a year
- No weekends
- Background check
- LMFT
- Psychiatry
- Paid holidays
- Health insurance
Quick Apply
Licensed Psychiatric Mental Health Nurse Practitioner
Headway —Winona, MN
- Up to $230 an hour
- Full-time
- Remote
- Private practice
- Psychiatry
- Mid-level
FT (20 appts/wk) Licensed Mental Health Therapist or Psychologist, PrivPrac, W2, Full Benefits
Affinity Psychological Services. P.C. —Saint Cloud, MN
- $5,100 - $9,200 a month
- Full-time
- Hybrid work
- Private practice
- LMFT
- Mid-level
- Continuing education credits
- Health insurance
Quick Apply
5d
Outpatient Mental Health Therapist
True Balance Ltd —Little Falls, MN
- $55,000 - $150,000 a year
- Part-time
- Background check
- Private practice
- LMFT
- Continuing education credits
- Health insurance
Quick Apply
Clinical Manager
BETHESDA HEALTH AND HOUSING —Willmar, MN
- $74,719.54 - $84,146.34 a year
- Weekends as needed
- CPR Certification
- Nursing
- RN License
Quick Apply
7d
Licensed Clinical Supervisor
ZUMBRO VALLEY HEALTH CENTER INC —Rochester, MN
- $68,307 - $85,000 a year
- Full-time
- LMFT
- Addiction Medicine
- Adults
- Free parking
- Continuing education credits
Quick Apply
9d

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Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available

Thermo Fisher Scientific -
Minnesota

Apply Now

Job Details

Full-time
$66,800 - $125,000 a year
4 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–$125,000.00.

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 associate jobs in minnesota

Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available

Manager, Clinical Initiatives - Remote

Senior Clinical Research Associate - CNS/Rare Disease - Central U.S. (Remote)

Behavioral Health Outpatient Therapist Clinical Trainee

Licensed Clinical Psychologist- IQ Testing

LPCC (Licensed Professional Clinical Counselor)

Licensed Mental Health Therapist

Licensed Mental Health Therapist

Treatment Supervisor, Full Time/Mental Health Professional

Licensed Clinical Psychologist

Licensed Mental Health Therapist

Licensed Mental Health Therapist

Licensed Clinical Assistant or Licensed Hygienist - Orthodontics

Clinical Systems Developer Lead

Mental Health Therapist or Social Worker

Licensed Psychiatric Mental Health Nurse Practitioner

FT (20 appts/wk) Licensed Mental Health Therapist or Psychologist, PrivPrac, W2, Full Benefits

Outpatient Mental Health Therapist

Clinical Manager

Licensed Clinical Supervisor

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