Site Clinical Specialist

Richfield, MN - USA

Monthly Salary: $ 27 - 33

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Thermo Fisher Scientific Inc. as a Site Clinical Specialist and be part of a team that is dedicated to driving world-class research! As a key player in the research community you will engage in impactful clinical trials involving patients or healthy volunteers. This role offers you the outstanding opportunity to contribute to groundbreaking studies and ensure the highest standards of patient safety and data integrity.

Responsibilities

Conduct multiple ongoing clinical trials according to FDA/GCP and ICH regulations and guidelines.
Provide medical care to patients prioritizing patient safety.
Schedule subject visits within protocol windows to increase scheduling capacity.
Perform all defined study activities including informed consent screening and protocol procedures such as vital signs pregnancy tests height weight and ECGs.
Record patient information and test results as per protocol on required forms.
Complete IP accountability logs and associated information where required.
Report suspected non-compliance to relevant site staff.
Ensure IRB approval is acquired prior to study initiation and maintain IRB requirements throughout the study.
Promote the company and build positive relationships with patients to ensure retention.
Attend site initiation meetings and other relevant meetings to receive protocol training.
Call patients book appointments and follow-up to confirm bookings or provide information/results.
Log and complete information on sponsor systems ensuring accuracy and timeliness.
Gather and maintain source documents updating patient files and notes with the most current information.
Adhere to company COP/SCOP.
Dispose of waste according to standards and assist in maintaining a neat facility.

Knowledge Skills and Abilities

Solid understanding of the clinical research process including GCP SOPs informed consent and safety monitoring.
Ability to work independently with attention to detail analyze complex information and solve problems.
Demonstrated discretion and good judgment.
Strong decision-making negotiation and influencing skills.
Effective communication skills and proficiency in English.
Good organizational abilities.
Proficiency in basic computer applications.
Strong interpersonal skills for teamwork.

Compensation and Benefits

The hourly pay range estimated for this position based in Minnesota is $27.00$33.00.

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: Experience:

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Thermo Fisher Scientific Inc. as a Site Clinical Specialist and be part of a team that is dedicated to driving world-class research! As a key player in the research community you will engage in impactful clinical trials...

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Responsibilities

Conduct multiple ongoing clinical trials according to FDA/GCP and ICH regulations and guidelines.
Provide medical care to patients prioritizing patient safety.
Schedule subject visits within protocol windows to increase scheduling capacity.
Perform all defined study activities including informed consent screening and protocol procedures such as vital signs pregnancy tests height weight and ECGs.
Record patient information and test results as per protocol on required forms.
Complete IP accountability logs and associated information where required.
Report suspected non-compliance to relevant site staff.
Ensure IRB approval is acquired prior to study initiation and maintain IRB requirements throughout the study.
Promote the company and build positive relationships with patients to ensure retention.
Attend site initiation meetings and other relevant meetings to receive protocol training.
Call patients book appointments and follow-up to confirm bookings or provide information/results.
Log and complete information on sponsor systems ensuring accuracy and timeliness.
Gather and maintain source documents updating patient files and notes with the most current information.
Adhere to company COP/SCOP.
Dispose of waste according to standards and assist in maintaining a neat facility.

Knowledge Skills and Abilities

Solid understanding of the clinical research process including GCP SOPs informed consent and safety monitoring.
Ability to work independently with attention to detail analyze complex information and solve problems.
Demonstrated discretion and good judgment.
Strong decision-making negotiation and influencing skills.
Effective communication skills and proficiency in English.
Good organizational abilities.
Proficiency in basic computer applications.
Strong interpersonal skills for teamwork.

Compensation and Benefits

The hourly pay range estimated for this position based in Minnesota is $27.00$33.00.

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: Experience:

Key Skills

Sales Experience
Crane
Customer Service
Communication skills
Heavy Equipment Operation
Microsoft Word
Case Management
OSHA
Team Management
Catheterization
Microsoft Outlook Calendar
EHS

Apply Now

About Company

Thermo Fisher Scientific

Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more

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