Showing posts with label Clinical. Show all posts
Showing posts with label Clinical. Show all posts
COORD CLINICAL RESEARCH II - Moffitt Cancer Center -  Tampa, FL

COORD CLINICAL RESEARCH II - Moffitt Cancer Center - Tampa, FL

Bachelor Degree Facilitates clinical research activity at Moffitt Cancer Center and/or affiliated institutions by entering data on to case report forms (CRF’s), and/or register data using remote data entry and/or electronic data entry. Coordinator will also assist with new patient eligibility evaluation, registration, and coordinating protocol-related care of patients enrolled on clinical trials. The clinical trials coordinator is responsible for collecting all source documentation and worksheets prepared by all members of the research team and then transcribing the data onto the appropriate collection tool for submission to the sponsor. The clinical trials coordinator is knowledgeable of protocol requirements and good clinical practices as set forth by Federal regulations. Provides data management support for the various research protocols. Maintains the day-to-day flow of data and forms pertaining to clinical research. Act as a resource for program protocols, the coordinator will act as a liaison between the investigators, primary care providers, Moffitt regulatory staff and the sponsor.
Moffitt Cancer Center - 1 day ago - save job - block The H. Lee Moffitt Cancer Center and Research Institute, founded in 1986, is a National Cancer Institute-designated Comprehensive Cancer Cen...

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Director Global Clinical Epidemiology (f/m)

Director Global Clinical Epidemiology (f/m)

¹Sie haben bei StepStone nach einem Job gesucht. Indem Sie Ihre E-Mail-Adresse eingeben, können Sie diese Suche speichern und regelmäßig passende Stellenangebote empfangen. Die Suche wird in Ihrem StepStone Account gespeichert, der automatisch für Sie erstellt wird. Dort können Sie Ihren Job Agent verwalten. Ihre Zugangsdaten erhalten Sie per E-Mail. Weitere Informationen erhalten Sie in unserer Datenschutzerklärung.

* Von Zeit zu Zeit können wir Ihnen, neben den von Ihnen abonnierten Karriere-Services, E-Mails zu ähnlichen Dienstleistungen von StepStone senden. Insofern Sie diese nicht erhalten möchten, klicken Sie bitte den Abmeldelink in der E-Mail oder melden Sie sich in Ihrem MyStepStone Account im Bereich „Nutzerdaten“ ab.


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Part-Time Medical Billing/Coding and Clinical Instructors - Volt Information Sciences - Elgin, IL

Part-Time Medical Billing/Coding and Clinical Instructors - Volt Information Sciences - Elgin, IL

Part-Time Medical Billing/Coding and Clinical Instructors more... ?

Part-Time Medical Billing/Coding and Clinical Instructors Posted on: 04/13/12 Job Number: 303186-8676-4-298741 Add to Cart Email to a Friend Location: Elgin , IL Description: We are currently looking for part-time evening medical billing and coding and clinical instructors for a career education institute in Elgin. The Instructors will lead at least 3 classes per day with 10-15 students. The Instructor's duties will include: *Teach and evaluate students in area of specialty *Prepare lesson plans, labs and assignments *Ability to adjust teaching style for diverse adult learners *Commitment to student learning and success *Design, administer and grade examinations Our client is a post-secondary education provider committed to quality, career-focused learning led by enthusiastic professionals who are inspired to transform an individual into a top-notch professional. They offer a variety of career and degree-granting programs in Information Technology, Healthcare and Business Administration career-oriented disciplines. Volt has been serving some of the nation's strongest companies for over 60 years. As a Volt employee, you can expect the highest level of on-site support. We have a long-standing tradition of developing lasting and mutually beneficial relationships with its employees.

Requirements: Certified coders and/or medical assistant certifications: RHIT/RHIA, RMA/CMA, CCA, CPC/CCS etc.. *Preferred at least 90 credits of undergraduate studies. * Minimum of 3 years of field experience. *Preferred at least 2 year of adult teaching or training experience in field of study. *Excellent platform and presentation skills. *Excellent communication skills (both written and oral) . *Strong organizational skills and attention to details. Volt is an equal opportunity employer.

Type: Contingent/Temporary Duration: 120 - 180 Days Payrate: $17.00 - $20.00 Hourly DOE Contact: Volt Workforce Solutions 311 S. Wacker Dr., Ste. 2300 Chicago, IL 60606 Phone: 312/994-65 Fax: 312/845-9075 (please use the apply button below)


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Part-Time Medical Billing/Coding and Clinical Instructors - Volt Information Sciences - Elgin, IL

Part-Time Medical Billing/Coding and Clinical Instructors - Volt Information Sciences - Elgin, IL

Part-Time Medical Billing/Coding and Clinical Instructors more... ?

Part-Time Medical Billing/Coding and Clinical Instructors Posted on: 04/13/12 Job Number: 303186-8676-4-298741 Add to Cart Email to a Friend Location: Elgin , IL Description: We are currently looking for part-time evening medical billing and coding and clinical instructors for a career education institute in Elgin. The Instructors will lead at least 3 classes per day with 10-15 students. The Instructor's duties will include: *Teach and evaluate students in area of specialty *Prepare lesson plans, labs and assignments *Ability to adjust teaching style for diverse adult learners *Commitment to student learning and success *Design, administer and grade examinations Our client is a post-secondary education provider committed to quality, career-focused learning led by enthusiastic professionals who are inspired to transform an individual into a top-notch professional. They offer a variety of career and degree-granting programs in Information Technology, Healthcare and Business Administration career-oriented disciplines. Volt has been serving some of the nation's strongest companies for over 60 years. As a Volt employee, you can expect the highest level of on-site support. We have a long-standing tradition of developing lasting and mutually beneficial relationships with its employees. Requirements: Certified coders and/or medical assistant certifications: RHIT/RHIA, RMA/CMA, CCA, CPC/CCS etc.. *Preferred at least 90 credits of undergraduate studies. * Minimum of 3 years of field experience. *Preferred at least 2 year of adult teaching or training experience in field of study. *Excellent platform and presentation skills. *Excellent communication skills (both written and oral) . *Strong organizational skills and attention to details. Volt is an equal opportunity employer. Type: Contingent/Temporary Duration: 120 - 180 Days Payrate: $17.00 - $20.00 Hourly DOE Contact: Volt Workforce Solutions 311 S. Wacker Dr., Ste. 2300 Chicago, IL 60606 Phone: 312/994-65 Fax: 312/845-9075 (please use the apply button below)

Industries: Media / Publishing Business Services


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Part-Time Medical Billing/Coding and Clinical Instructors - Volt Information Sciences - Elgin, IL

Part-Time Medical Billing/Coding and Clinical Instructors - Volt Information Sciences - Elgin, IL

Part-Time Medical Billing/Coding and Clinical Instructors more... ?

Part-Time Medical Billing/Coding and Clinical Instructors Posted on: 04/13/12 Job Number: 303186-8676-4-298741 Add to Cart Email to a Friend Location: Elgin , IL Description: We are currently looking for part-time evening medical billing and coding and clinical instructors for a career education institute in Elgin. The Instructors will lead at least 3 classes per day with 10-15 students. The Instructor's duties will include: *Teach and evaluate students in area of specialty *Prepare lesson plans, labs and assignments *Ability to adjust teaching style for diverse adult learners *Commitment to student learning and success *Design, administer and grade examinations Our client is a post-secondary education provider committed to quality, career-focused learning led by enthusiastic professionals who are inspired to transform an individual into a top-notch professional. They offer a variety of career and degree-granting programs in Information Technology, Healthcare and Business Administration career-oriented disciplines. Volt has been serving some of the nation's strongest companies for over 60 years. As a Volt employee, you can expect the highest level of on-site support. We have a long-standing tradition of developing lasting and mutually beneficial relationships with its employees. Requirements: Certified coders and/or medical assistant certifications: RHIT/RHIA, RMA/CMA, CCA, CPC/CCS etc.. *Preferred at least 90 credits of undergraduate studies. * Minimum of 3 years of field experience. *Preferred at least 2 year of adult teaching or training experience in field of study. *Excellent platform and presentation skills. *Excellent communication skills (both written and oral) . *Strong organizational skills and attention to details. Volt is an equal opportunity employer. Type: Contingent/Temporary Duration: 120 - 180 Days Payrate: $17.00 - $20.00 Hourly DOE Contact: Volt Workforce Solutions 311 S. Wacker Dr., Ste. 2300 Chicago, IL 60606 Phone: 312/994-65 Fax: 312/845-9075 (please use the apply button below)

Industries: Media / Publishing Business Services


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McKESSON HED CLINICAL CONSULTANT - ()

McKESSON HED CLINICAL CONSULTANT - ()

Dell believes technology helps people and communities to grow and succeed. That’s why we empower you to always think ahead, giving you the tools and the training to keep attaining new levels of success for you and for our customers.

When you join Dell in North America, you’re free to be inventive, delivering solutions that make a real difference in people’s lives. Your teams will be rewarded for curiosity and for bringing different perspectives to the table. And there will always be opportunities for you to learn, to grow, and to succeed while you bring new solutions to our customers.

You’ll invent world-class ideas that solve our customers’ tough problems every day when you join Dell in North America. Let’s see what we can dream up together.


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Clinical Trial Coordinator

Clinical Trial Coordinator

WE ARE LOOKING FOR

We are looking for a Clinical Trial Coordinator with the desire to participate in conducting

clinical investigations with medical devices in Europe. If you have a proven “can do”

attitude and you like working in an international environment, you might be interested

in the position.

JOB PROFILE

In Clinical Research, we are responsible for coordinating clinical studies together with

our US-based counterpart. As part of a transatlantic clinical project team, you will get

the opportunity to participate in managing the European part of the investigations

from start to end. We have investigations within the SBUs Peripheral Intervention and

Endoscopy. You must be willing and able to travel.

Your responsibilities as a Clinical Trial Coordinator will be to:

Help submitting clinical documents to Competent Authorities and Ethics Committees to obtain approvalsTrain sites in Electronic Data Capturing SystemHelp provide clinical study agreements, carry out safety reporting, coordinate investigational devices, create notes to files, and reimburse the sitesEstablish close working relationships with physicians, their research staffs, and outside consultants through exceptional communication on a regular basisAssist the Clinical Project Leader in conducting meetings with investigative sites, physicians, and consultantsArchive study related documents in coordination with team membersRespond promptly and appropriately to study issues raised by investigative sites, sponsors, monitors, and consultants.JOB PROFILE

We are looking for a colleague with good interpersonal skills. It is obvious that you

work independently with your own responsibilities and thrive on an international

dynamic environment.

As a Clinical Trial Coordinator, we also expect you to have the following qualifications:

A Nursing degree or a Masters degree in Health, Life Science, or Biomedical EngineeringWorking knowledge of ISO 14155, MDD, FDA, and other regulatory requirementsPreferably experience in conducting clinical investigationsExperience in using Electronic Data Capturing SystemExcellent communication skills and fluency in verbal and written EnglishWE OFFER

Cook Medical has a healthy company culture with a strong common set of values, and

responsible, competent and professional staff is our most important resource. We have

a flat organizational structure with the focus on open dialogue. Qualities such as determination,

loyalty and humor are highly appreciated.

The staff of Cook Medical helps to uphold the company’s philosophy of developing

innovative medical solutions to raise the quality of patient treatment worldwide - we

make a difference!

ADDITIONAL INFORMATION

For further information about the position, please contact Susanne Holm Faarbæk,

Clinical Manager, on +45 56 86 86 86 or e-mail Susanne.Faarbaek@cookmedical.com

APPLICATION LETTER

Please send your application letter and CV (both in English) to Anne-Mette Vangkilde,

HR Generalist, by August, 10.

You may also e-mail your application to job@cook-wce.com .

COMPANY PROFILE

Cook Medical is a leader in researching, developing and manufacturing medical technologies that improve quality of life for people around the world. To provide our customers with the best possible support, we have nine strategic business units (SBUs) that each specializes in a particular segment of medicine. Products are manufactured on three continents and are distributed to 135 countries. In Denmark, we currently employ around 650 people.

William Cook Europe, Sandet 6, 4632 Bjæverskov, Denmark


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Clinical Coding and Documentation Specialist - E/M Coding - ... - IPC: The Hospitalist Company - N Hollywood, CA

Clinical Coding and Documentation Specialist - E/M Coding - ... - IPC: The Hospitalist Company - N Hollywood, CA

Clinical Coding and Documentation Specialist - E/M Coding - CPC - CCS more... ?

IPC, The Hospitalist Company, has an immediate opening for a Clinical Coding and Documentation Specialist in North Hollywood, CA.

The primary purpose and function of the Clinical Coding and Documentation Specialist is to assist Physician Providers with Education and Management on a variety of data sources to determine where intervention with providers is needed, and formulate and implement a provider intervention plan.

Typically, an intervention plan will include provider re-education, additional auditing or other corrective action.

Data sources include audit results, coding analyses, and payer reimbursement findings.Founded by physicians in 1995, IPC The Hospitalist Company has grown to become the nation?s leading private practice hospitalist group.

Our providers, support staff, operations, and technology are all focused on driving the health care delivery system towards better, more efficient and high quality inpatient care.

Today, we manage over 150 practice groups, providing care in over 500 medical facilities in 21 states.Why work for us: Industry leader and innovatorA competitive compensation and benefits package Professional advancement and career growth opportunitiesA team structure that fosters mutual respect Benefits: The following benefits are offered to full-time team members.Medical Insurance Dental Insurance Life Insurance Long-Term Disability Insurance Section 125 Health Savings Account 401(k) Retirement Plan, with employer match Employee Stock Purchase Plan Paid Time Off And more!About UsIPC The Hospitalist Company, INC.

is a publicly held leading national physician group practice company focused on the delivery of hospitalist medicine services.

Our physicians and affiliated providers manage the care of hospitalized patients in coordination with primary care physicians and specialists.We have taken a leadership role in the emergence of this new medical specialty and today has over 1400 affiliated providers in the U.S.

We work closely with approximately 30,0 referring primary care physicians and specialists and more than 1,0 health plans, to manage more than $1 billion in healthcare expenditures annually.

On January 24, 2008, we became the first practice group exclusively focused on hospital medicine to become a publicly traded company.Are You Passionate About What You Do? Apply Today!Requirements: Responsibilities: Review a variety of data sources to determine where intervention with providers is needed.

Data sources include documentation audit results, coding analyses, payer reimbursement findings, provider or staff inquiries or concerns, Compliance Hot Line reports, and others Formulate and implement an intervention plan.Perform provider and/or staff education Actively participate in Compliance Committees, task forces, or other work groups Prepare summary reports of activities and present at the appropriate Compliance Committee Meeting Provide coding & documentation support to the Centralized Billing Officer when responding to payer concerns Coordinate Internal Investigations related to coding, documentation, or billing issues, and manage the Investigation process so that appropriate investigation and corrective action occur Research payer, regulator, and legislative information to determine correct approach to specific coding & documentation issues.

Create educational handouts or materials as necessary, and disseminate information to end users Assist in Charge Master maintenance by reviewing CPT/HCPCS codes and ensuring that services provided are correctly reflected on the Charge Master.

Update Charge Master as needed, and conduct annual review Other projects as assigned Requirements: E&M coding/documentation in acute care and or SNF/NF care strongly preferred Bachelors Degree required Certified Coder required, CPC or CCS Physician Coding Certificate (CPC-P, CCS-P, CEMC)3 years experience Education and Management Coding ? E&M Expertise in Medicare and Medicaid requirements Expertise in reviewing physician documentation of E&M services Additional healthcare compliance certification preferred (CHC, CCP)


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Manager, Clinical Research Job

Manager, Clinical Research Job

Manager, Clinical Research

Job ID 80420
Location: US-PA-Pittsburgh Area

Experience Level: Not Indicated
Education Level: Other
Type of Function: Full-Time Regular
Travel Percentage: 0

Organization Description:
We simplify healthcare by focusing on the people in the care cycle – patients and care providers. Through combining human insights and clinical expertise, we aim to improve patient outcomes while lowering the burden on the healthcare system. Philips delivers advanced solutions for both health professionals, to meet the needs of patients, and empowered consumers for affordable healthcare whether in hospital or at home.

Some product highlights: 256-slice Brilliance iCT scanner, Integrated cath lab, Avalon FM 20 & FM 30 fetal monitors, Ambient Experience MR and CT systems, Philips Lifeline's personal emergency alert service.

To support Philips Home Health Solutions (HHS) / Sleep and Respiratory Care (SRC) Business Units (BU’s) and external customers by managing the successful design, planning, and implementation of quality scientific clinical research that results in data which are timely, and of high quality and integrity, to support Engineering, Regulatory or Marketing needs.

Your Responsibilities:
- Accountable to ensure the timely and accurate completion of all clinical studies (US and international), the compilation of all study data and reports to support regulatory submissions, product documentation and publications
- Attend FDA or other regulatory meetings in support of submissions with clinical data or needs
- Demonstrated proficiency in scientific writing in relevant content areas. Write and edit scientific clinical trial protocols
- Develop and effectively manage relationships (liaison) with key opinion leaders (KOLs), BU leads and executive team members
- Manage financial budgets associated with execution of clinical activities and departmental operations
- Ensure adherence to Quality System Procedures (QSPs) and that all research processes and procedures are state of the art and meet all regulatory requirements. Review and revised as indicated
- Oversee or coordinate departmental or site quality audits
- Manage and mentor clinical associates, ensure professional development and succession planning, conduct performance reviews for direct reports
- Routinely assess performance of the clinical team through a customer satisfaction survey and act on findings

Key Challenges:
- Managing associates who are responsible for multiple projects and tasks
- Establishing and updating priorities
- Achieving goals within annual operating plan
- Adapting in a dynamic business environment
- Developing and maintaining KOL network
- Effective and timely communication

Your Profile:
- Bachelor of Science degree in a scientific or health care field required. Masters of Science degree or higher (preferred)
- Demonstrated scientific writing abilities
- Strong understanding of biostatistics
- Experience:
- Minimum of 5 years of clinical research experience preferably in the medical device industry or field of sleep medicine
- Minimum of 5 years of supervisory/ leadership experience preferred
- Working knowledge of Good Clinical Practices (GCP’s); and US / international clinical research regulations
- Effective oral and written communication skills at multiple levels (e.g. associates, executives, physicians)
- Effective interpersonal skills
- Demonstrated efficiency with common office computer software, e-mail, and data management programs.

* Contacts: Philips

Notes
Philips is an Equal Opportunity Employer


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Clinical Coding Specialist - Renown South Meadows Medical Center - Reno, NV

Clinical Coding Specialist - Renown South Meadows Medical Center - Reno, NV

Clinical Coding Specialist more... ?
Renown South Meadows Medical CenterSeptember 22, 2010 (last updated 30+ days ago)

Clinical Coding Specialist
Department: 400736 Health Information Mgt
Facility: Renown South Meadows Medical Center
Reno, NV
Schedule: Full Time - Eligible for Benefits
Shift: Day
Hours: 0800-1630

Job Details:
*

Position Purpose:
The purpose of this position is to apply the appropriate diagnostic and procedure codes to individual patient health information for data retrieval, analysis, and claims processing.

Nature and Scope:
A clinical coding specialist reviews and analyzes health records to identify relevant diagnoses and procedures for distinct patient encounters. The coding specialist is responsible for translating diagnostic phrases utilized by healthcare providers into coded form. The translation process required interaction with the healthcare provider to ensure that the terms have been translated correctly. The coded information that is a product of the coding process is then utilized for reimbursement purposes, in the assessment of clinical care, to support medical research activity, and to support the identification of healthcare concerns critical to the public at large.

The clinical coding specialist must have a thorough understanding of the content of the medical record in order to be able to locate information to support or provide specificity for coding. The coder must be trained in the anatomy and physiology of the human body and disease processes in order to understand the etiology, pathology, symptoms, signs, diagnostic studies, treatment modalities, and prognosis of diseases and procedures to be coded. The coding specialist works as a part of a team to achieve the best quality patient care.

This position is challenged to be aware of the continual changes in Federal and State regulations for prospective payment, keep informed of changes in treatment modes and new procedures, and to perform coding when physician documentation is vague or missing.

Incumbent must consistently meet or exceed productivity and quality standards as defined in the job description.

KNOWLEDGE, SKILLS & ABILITIES

1. Knowledge of ICD9-CM, CPT and HCPCS coding.
2. Conversion of written description to proper billing codes.
3. Ability to appeal CPT and ICD-9-CM for maximum reimbursement.
4. Comprehension of disease processes.
5. Ability to work well with others.
6. Medical Records content standards.
7. Philosophy consistent with Standards of Conduct.

This position does notprovide patient care.

The foregoing description is not intended and should not be construed to be an exhaustive list of all responsibilities, skills and efforts or work conditions associated with the job. It is intended to be an accurate reflection of the general nature and level of the job.

Minimum Qualifications: Requirements - Required and/or Preferred

Education:
Must have working-level knowledge of the English language, including reading, writing and speaking English. Bachelor Degree in Health Information Management preferred.

Experience:
A minimum of one (1) year of previous inpatient and outpatient in an acute care facility is required but three (3) years of previous experience is preferred.

License (s):
None
Certification (s):
CCS, RHIT or RHIA required.

Computer / Typing:
Must possess, or be able to obtain within 90 days, the computers skills necessary to complete online learning requirements for job-specific competencies, access online forms and policies, complete online benefits enrollment, etc.

Industries: Hospital / Healthcare


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Clinical Coding Specialist - Renown South Meadows Medical Center - Reno, NV

Clinical Coding Specialist - Renown South Meadows Medical Center - Reno, NV

Clinical Coding Specialist more... ?
Renown South Meadows Medical CenterSeptember 22, 2010 (last updated 30+ days ago)

Clinical Coding Specialist
Department: 400736 Health Information Mgt
Facility: Renown South Meadows Medical Center
Reno, NV
Schedule: Full Time - Eligible for Benefits
Shift: Day
Hours: 0800-1630

Job Details:
*

Position Purpose:
The purpose of this position is to apply the appropriate diagnostic and procedure codes to individual patient health information for data retrieval, analysis, and claims processing.

Nature and Scope:
A clinical coding specialist reviews and analyzes health records to identify relevant diagnoses and procedures for distinct patient encounters. The coding specialist is responsible for translating diagnostic phrases utilized by healthcare providers into coded form. The translation process required interaction with the healthcare provider to ensure that the terms have been translated correctly. The coded information that is a product of the coding process is then utilized for reimbursement purposes, in the assessment of clinical care, to support medical research activity, and to support the identification of healthcare concerns critical to the public at large.

The clinical coding specialist must have a thorough understanding of the content of the medical record in order to be able to locate information to support or provide specificity for coding. The coder must be trained in the anatomy and physiology of the human body and disease processes in order to understand the etiology, pathology, symptoms, signs, diagnostic studies, treatment modalities, and prognosis of diseases and procedures to be coded. The coding specialist works as a part of a team to achieve the best quality patient care.

This position is challenged to be aware of the continual changes in Federal and State regulations for prospective payment, keep informed of changes in treatment modes and new procedures, and to perform coding when physician documentation is vague or missing.

Incumbent must consistently meet or exceed productivity and quality standards as defined in the job description.

KNOWLEDGE, SKILLS & ABILITIES

1. Knowledge of ICD9-CM, CPT and HCPCS coding.
2. Conversion of written description to proper billing codes.
3. Ability to appeal CPT and ICD-9-CM for maximum reimbursement.
4. Comprehension of disease processes.
5. Ability to work well with others.
6. Medical Records content standards.
7. Philosophy consistent with Standards of Conduct.

This position does notprovide patient care.

The foregoing description is not intended and should not be construed to be an exhaustive list of all responsibilities, skills and efforts or work conditions associated with the job. It is intended to be an accurate reflection of the general nature and level of the job.

Minimum Qualifications: Requirements - Required and/or Preferred

Education:
Must have working-level knowledge of the English language, including reading, writing and speaking English. Bachelor Degree in Health Information Management preferred.

Experience:
A minimum of one (1) year of previous inpatient and outpatient in an acute care facility is required but three (3) years of previous experience is preferred.

License (s):
None
Certification (s):
CCS, RHIT or RHIA required.

Computer / Typing:
Must possess, or be able to obtain within 90 days, the computers skills necessary to complete online learning requirements for job-specific competencies, access online forms and policies, complete online benefits enrollment, etc.

Industries: Hospital / Healthcare


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Clinical Trial Coordinator

Clinical Trial Coordinator

WE ARE LOOKING FOR

We are looking for a Clinical Trial Coordinator with the desire to participate in conducting

clinical investigations with medical devices in Europe. If you have a proven “can do”

attitude and you like working in an international environment, you might be interested

in the position.

JOB PROFILE

In Clinical Research, we are responsible for coordinating clinical studies together with

our US-based counterpart. As part of a transatlantic clinical project team, you will get

the opportunity to participate in managing the European part of the investigations

from start to end. We have investigations within the SBUs Peripheral Intervention and

Endoscopy. You must be willing and able to travel.

Your responsibilities as a Clinical Trial Coordinator will be to:

Help submitting clinical documents to Competent Authorities and Ethics Committees to obtain approvalsTrain sites in Electronic Data Capturing SystemHelp provide clinical study agreements, carry out safety reporting, coordinate investigational devices, create notes to files, and reimburse the sitesEstablish close working relationships with physicians, their research staffs, and outside consultants through exceptional communication on a regular basisAssist the Clinical Project Leader in conducting meetings with investigative sites, physicians, and consultantsArchive study related documents in coordination with team membersRespond promptly and appropriately to study issues raised by investigative sites, sponsors, monitors, and consultants.JOB PROFILE

We are looking for a colleague with good interpersonal skills. It is obvious that you

work independently with your own responsibilities and thrive on an international

dynamic environment.

As a Clinical Trial Coordinator, we also expect you to have the following qualifications:

A Nursing degree or a Masters degree in Health, Life Science, or Biomedical EngineeringWorking knowledge of ISO 14155, MDD, FDA, and other regulatory requirementsPreferably experience in conducting clinical investigationsExperience in using Electronic Data Capturing SystemExcellent communication skills and fluency in verbal and written EnglishWE OFFER

Cook Medical has a healthy company culture with a strong common set of values, and

responsible, competent and professional staff is our most important resource. We have

a flat organizational structure with the focus on open dialogue. Qualities such as determination,

loyalty and humor are highly appreciated.

The staff of Cook Medical helps to uphold the company’s philosophy of developing

innovative medical solutions to raise the quality of patient treatment worldwide - we

make a difference!

ADDITIONAL INFORMATION

For further information about the position, please contact Susanne Holm Faarbæk,

Clinical Manager, on +45 56 86 86 86 or e-mail Susanne.Faarbaek@cookmedical.com

APPLICATION LETTER

Please send your application letter and CV (both in English) to Anne-Mette Vangkilde,

HR Generalist, by August, 10.

You may also e-mail your application to job@cook-wce.com .

COMPANY PROFILE

Cook Medical is a leader in researching, developing and manufacturing medical technologies that improve quality of life for people around the world. To provide our customers with the best possible support, we have nine strategic business units (SBUs) that each specializes in a particular segment of medicine. Products are manufactured on three continents and are distributed to 135 countries. In Denmark, we currently employ around 650 people.

William Cook Europe, Sandet 6, 4632 Bjæverskov, Denmark


View the original article here

Kategori

Kategori