Top 174 Investigator Jobs in Frisco, Tx

Clinical Affairs Specialist III
Integer Holdings Corporation —Plano, TX
- Full-time
- Nursing
- Oracle
- 3 years
- Disability insurance
- Health insurance
Quick Apply
Research Project Mgr
Baylor Scott & White Health —Plano, TX
- Mid-level
- Master's degree
- Bachelor's degree
- Health insurance
- Tuition reimbursement
13d
Criminal Investigator
RealPage, Inc. —Richardson, TX
- $26.97 - $45.91 an hour
- Background check
- Mid-level
- Windows
- Paid holidays
- Dental insurance
Investigator (226 Days)
Dallas Independent School District —Dallas, TX
- $65,522 - $79,914 a year
- Full-time
- Writing skills
- Mid-level
- Office
3d
Manager, Fraud and Investigations
Public Storage —Frisco, TX
- Full-time
- 7 years
- Analysis skills
- US work authorization
Quick Apply
2d
Auditor/Investigator II
Qlarant —Dallas, TX
- $57,512 - $85,839 a year
- Full-time
- Mid-level
- Analysis skills
- Bachelor's degree
Quick Apply
Financial Crimes Compliance Operations, Analyst
MUFG —Irving, TX
- $70,000 - $82,000 a year
- Full-time
- Hybrid work
- Background check
- Research
- Mid-level
- Paid parental leave
- Paid holidays
3d
Multifamily Underwriting Fraud Investigation - Lead Associate
Fannie Mae —Plano, TX
- $109,000 - $142,000 a year
- Full-time
- Hybrid work
- Office
- Analysis skills
- Bachelor's degree
Senior Associate Relations Investigator
GEICO —Richardson, TX
- Full-time
- 3 years
- Continuous improvement
- Psychology
10d
Unregulated Operations Investigator IV
Health & Human Services Comm —Dallas, TX
- $5,368.08 - $6,779.25 a month
- Weekends as needed
- Background check
- Office
- Driver's License
- Health insurance
- Opportunities for advancement
Quick Apply
HR Advisor
GEICO —Richardson, TX
- Full-time
- Mid-level
- Bachelor's degree
- Continuous improvement
10d
Research Enrollment Anlst
Baylor Scott & White Health —Dallas, TX
- Microsoft Excel
- Quality control
- Data entry
- Health insurance
- Tuition reimbursement
3d
LP Investigator-based out of Whiterock, Texas
Shoe Carnival —Dallas, TX
- $75,000 a year
- Full-time
- 5 years
- High school diploma or GED
- Supervising experience
- Employee stock purchase plan
- Health insurance
Quick Apply
drug safety and pharmacovigilance
Sally Health & Innovative Partners —Dallas, TX
- $150,000 - $200,000 a year
- Full-time
- Hybrid work
- Doctoral degree
- Senior level
- Health insurance
- Dental insurance
Quick Apply
Litigation Case Investigator
KDC LLC —Dallas, TX
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- AD&D insurance
- Paid holidays
Quick Apply
4d
Transaction Monitoring Investigator
Guidehouse Managed Services LLC —Lewisville, TX
- Full-time
- Research
- Mid-level
- Office
- Health savings account
- Paid holidays
Pre-Litigation Case Investigator
KDC LLC —Dallas, TX
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Research
- AD&D insurance
- Paid holidays
Quick Apply
CounterIntelligence Data Exfiltration Investigator -
Raytheon —McKinney, TX
- $107,500 - $204,500 a year
- Full-time
- 5 years
- Bachelor of Science
- Office
- Paid holidays
- Disability insurance
INVESTIGATIVE SPECIALIST (INVESTIGATIONS) (FULL TIME)
City of Richardson, TX —Richardson, TX
- $45,457 - $52,276 a year
- Full-time
- Background check
- Construction site
- Word processing
Associate Relations Supervisor
GEICO —Richardson, TX
- $86,100 - $141,450 a year
- Full-time
- Mid-level
- Bachelor's degree
- Quality control
10d

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Clinical Affairs Specialist III

Integer Holdings Corporation -
Plano, TX

Quick Apply

Job Details

Full-time

Benefits

Disability insurance
Health insurance
Dental insurance
Paid time off
Adoption assistance
Parental leave
Vision insurance
401(k) matching
Life insurance

Qualifications

Product development research management
Data integrity assurance
Medical writing
Nursing
Content creation for technical audiences
Oracle
Safety protocol adherence
Team leadership
Technical documentation
Clinical staff development programs
Critical literature reviews
3 years
Minitab
Clinical audit and monitoring
Data integrity and documentation
Collaboration with product development teams
ICH guidelines
Clinical staff training
Product development projects
Budget planning
Technology management
Clinical training
Pharmaceutical company experience
Health information data integrity
Data quality monitoring
Clinical program monitoring
Health Science
Clinical data report preparation
Organizational skills
Technology budget management

Full Job Description

By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success.

At Integer, our values are embedded in everything we do.

Customer

We focus on our customers’ success

Innovation

We create better solutions

Collaboration

We create success together

Inclusion

We always interact with others respectfully

Candor

We are open and honest with one another

Integrity

We do the right things and do things right

You will adhere to Integer Core Beliefs and Values all safety, environmental, security and quality
requirements including, but not limited to: Quality Management Systems ( Safety, Environmental and
Security Management Systems, U.S. Food and Drug Administration ( regulations, company policies
and operating procedures, and other regulatory requirements.
You will contribute to global clinical strategies to support clinical evidence requirements for product
submissions and post submission activities.
You will represent the Clinical Affairs function on product development teams.
You will work directly with representatives from cross functional areas in possibly multiple geographical locations
You will ensure clinical data integrity in support of the quality and regulatory functional group needs. This will include the use of software to appraise, analyse and evaluate clinical and state of the art data to generate appropriate clinical evidence to support Integer Technologies
You will generate interim and final reports.
You will support Integer initiatives with the development and upkeep of market specific clinical training.
You will support investigator conferences to review findings and advise on direction.
You will interface with, and assure training of investigators/physicians, centre staff and Integer Clinical
Affairs staff.
You will support adequate monitoring is conducted on all clinical trials.
You will provide a clinical perspective and approval on field complaint investigations
You will work with regulatory bodies for the purpose of facilitating regulatory approvals and queries.
You will s upport the development of Integer technology including objectives, strategy, scope, budget, and schedule from proof of concept research, development through post market commercial phases
You will perform other functions as required.

How you will be measured:

The specific measures listed below may be subject to change and are not intended to be an all inclusive list
Safety is our highest priority; you will be an active supporter of the Integer Environmental, Health
Safety programs and the specific behavior based safety programs
You will have defined Goals and Objectives specifying key projects and expected milestones to achieve.
Ensure clinical data arguments provided in clinical evaluation documents are sufficient to support regulatory product approvals
Support revenue growth by leveraging clinical knowledge to support the growth team initiatives
The creation of market specific clinical training
Ensure documentation and data are maintained to reflect State of the Art
Ensure State of the Art clinical processes are maintained and continuously underpinned by current knowledge and insight gained
Support the Development and maintenance of the physician advisory board to and its functions as directed
Cost You will be expected to complete clinical inputs for product approval and product renewal within budget
On Time Delivery particularly those that are impacted by the results of projects that you are involved in, and deliver ed by specified milestones
Your expertise coupled with your accomplishments and collaboration with others to deliver
results will also be considered.

What sets you apart:

You have a degree from higher education (Science, Engineering, Health Science, Nursing or related field
You have 3 years of documented professional experience; or 5-7 years of documented professional experience if a degree is not a prerequisite for a given task.
You have experience in medical device industry or pharmaceutical industry including US and international medical device regulatory submissions/approvals.
You have experience with implantable devices and/or other high risk device types.
You are suitably qualified as per MEDDEV 2.7.1 (rev 4), section 6.4 with experience of research methods, information management, literature reviews and technical writing.
You have knowledge and experience of clinical evaluations.
You have knowledge and experience with various medical device regulations such as the Medical Device Regulation (2017/ 21 CFR Part 812, and standards guidance documents such as MEDDEV 2.7.1 (rev 4) MDCG 2020 5, MDCG 2020 6, ICH Guidelines and their application
You have experience working with the medical community including physicians.
You have knowledge of feasibility, pivotal and post market clinical trials.
You can work independently as well as collaboratively within the organization.
You have developed good written and oral communication skills. This includes the ability to assist in teaching and training less experienced or knowledgeable associates. Clear and professional communications to all levels of the organization are important in this role
You have experience working in ERP systems, (such as Oracle, Reliance, etc.), Minitab, Excel, etc.
You have leadership skills with demonstrated ability to drive positive results and deliver projects on time for deliverables and within budget.

Salary range $75,750 - $111,00

#IND1

Our total rewards program is designed to attract, retain, and motivate associates to contribute to Integer’s success. Our compensation program includes base salary and a cash-based incentive program supporting our pay-for-performance philosophy. We provide a comprehensive benefits package with immediate eligibility including medical, dental, vision, disability, life insurance, and adoption benefits. Parental leave is available after one year. Optional employee-paid programs include supplemental life insurance, critical illness, hospital indemnity and accident insurance. Employees are immediately eligible to participate in the 401(k) plan with company matching contributions. We provide 80 hours (10 days) of company designated holidays per year plus an annual allotment of paid time off.

U.S. Applicants: Equal Opportunity Employer. In addition, veterans and individuals with disabilities are encouraged to apply.

Quick Apply

Refine Your Search

investigator jobs in frisco, tx

Clinical Affairs Specialist III

Research Project Mgr

Criminal Investigator

Investigator (226 Days)

Manager, Fraud and Investigations

Auditor/Investigator II

Financial Crimes Compliance Operations, Analyst

Multifamily Underwriting Fraud Investigation - Lead Associate

Senior Associate Relations Investigator

Unregulated Operations Investigator IV

HR Advisor

Research Enrollment Anlst

LP Investigator-based out of Whiterock, Texas

drug safety and pharmacovigilance

Litigation Case Investigator

Transaction Monitoring Investigator

Pre-Litigation Case Investigator

CounterIntelligence Data Exfiltration Investigator -

INVESTIGATIVE SPECIALIST (INVESTIGATIONS) (FULL TIME)

Associate Relations Supervisor

I want to receive the latest job alert for investigator in frisco, tx

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