Clinical Quality Specialist

Position: Clinical Documentation Specialist Grade: Reporting To: Team Manager Department: CARE - Virtual Scribe Profile Description: This role would be responsible for creating medicolegally compliant, clinically sound, high quality outpatient visit documentation for some of the best US Hospitals across multiple specialties on the electronic platform. ...

**JD of Quality Assurance** **General Information** **Designation: Quality Assurance** **Status: Full-time** - In depth knowledge regarding Clinical trial processes, drug discovery life cycle, and computer systems used in clinical Sciences. - Ability to understand life sciences and healthcare regulatory reporting and compliance. - Experience in working on...

**JD of Quality Assurance** **General Information** **Designation: Quality Assurance** **Status: Full-time** - In depth knowledge regarding Clinical trial processes, drug discovery life cycle, and computer systems used in clinical Sciences. - Ability to understand life sciences and healthcare regulatory reporting and compliance. - Experience in working on...

Main role of the scribe is to create medicolegally compliant, clinically sound high quality outpatient visit documentation for some of the best US Hospitals across multiple specialties . Listen and comprehend recorded patient physician interactions, develop an impression about the clinical condition and document clinical history, examination findings &...

Are you passionate about helping patients overcome musculoskeletal challenges and contributing to their well-being? QI Spine Clinic, India's premier chain of Spine Rehabilitation clinics, is seeking dedicated **Physiotherapists** to join our expert team. Ranked #1 in 5 major cities by Times Of India Survey for 2 consecutive years, we offer a unique...

Clinical Database Programmer Bachelor’s Degree (Science, Pharmacy, Life science, Computer Application), with minimum Four to five years of experience in Clinical Data Management. Experience in MS Office; additional Certification in MS-Office or Microsoft Office Specialist (MOS) certification will be an asset. Familiarity with Medical Terminology;...

3M has a long-standing reputation as a company committed to innovation. We provide the freedom to explore and encourage curiosity and creativity. We gain new insight from diverse thinking, and take risks on new ideas. Here, you can apply your talent in bold ways that matter. Job Description: Summary: Function as “Clinical Specialist” in the...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1 . Trial...

Associate Clinical Data Processor Bachelor’s Degree in any stream or Final Year Appeared with zero to one year of experience in performing data entry activities. Experience in MS Office; additional Certification in MS-Office or Microsoft Office Specialist (MOS) certification will be an asset. Ability to read, write and speak in English; English proficiency...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1.Trial...

Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process. Responsibilities: 1 . Trial...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1.Trial...

About the job At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience and integrity come together to advance the state of clinical development. Senior Clinical Programmer (Quality/Technical Review) role...

**Enhance your reach for an exciting opportunity in QI Spine as a Spine Specialist.** **QI Spine Clinic, India's first chain of clinics dedicated to Spine Rehabilitation by an expert team of Spine Specialists ranked #1 in 4 cities by Times Of India Survey for 2 Consecutive Years 2018 in Mumbai, Delhi, Gurgaon, Bangalore and Pune.** **Responsibilities and...

105,000 people reimagining medicine for more than 766 million people globally. To provide country clinical strategic guidance and feasibility assessment for GDD trials. Your responsibilities include, but are not limited to - To provide clinical strategic and tactical leadership in the country to support GDD trials, clinical development plans which change the...

MissionWe are seeking a diligent Quality Assurance Specialist to oversee the procedures andstandards for our sales/support unit. The successful candidate will monitor calls,emails, and other types of customer interactions to ensure that high standards ofquality are being met and compliance with policies is maintained.Responsibilities- Evaluate customer...

o To meet all the inpatients on daily basis during the regular ward visits. - To plan the diets according to the patient’s medical condition. - To initiate the nutrition care process by way of performing nutrition screening that identifies patients at Nutrition risk. - To do the re-assessment or monitor the prognosis of all the patients who are at...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...