Clinical Associate-obgy

Hiring - Clinical Assistant OBGY Min 1 year experience in OBGY Location Pune BAMS+MS/DGO/CGO **Salary**: ₹28,000.00 - ₹35,000.00 per month **Benefits**: - Health insurance Schedule: - Rotational shift Ability to commute/relocate: - Pune, Maharashtra: Reliably commute or planning to relocate before starting work (required) **Experience**: -...

Qualification: BAMS + MS (OBGY) Location: Pune Experience: 2 Years to 3 Years

Urgent hiring Clinical Associate-Gynec for reputed multispeciality hospital in Pune. Qualification : MBBS+DGO/ DNB with valid Maharashtra Medical Council/ MCI Registration is required. Experience : 2+ years relevant experience in OBGY with 50+ beded multispeciality hospital is required. Salary : Rs.70,000/- to Rs.1,20,000/- (Subject to Qualification,...

Established in 2007, Jupiter Hospital is a tertiary and quaternary healthcare hospital that lays its foundation on a ‘Patient first’ ideology. Our mission is to create the best infrastructure, technology and support to put Patient First & foremost and be futuristic, innovative in delivery of healthcare. We are looking for a Clinical Associate with 2-4...

**Job Overview**: **Clinical Associate - NICU /PICU- MBBS PLUS DGO/DNB/ MS**: **Pune**: - Job Location:Baner - Experience:3-4 years - Salary: 90k to 1.2lacs - Job Type:Full Time - Work Location: - No of vacancies:2 **Required Skills**: Clinical Associate - NICU /PICU- MBBS PLUS DGO/DNB/ MS EXP - 1to 4years exp obgy salary - 90k to 1.2lacs contact - ...

Urgent hiring Clinical Associate-Gynec for reputed multispeciality hospital in Pune.Qualification : MBBS+DGO/ DNB with valid Maharashtra Medical Council/ MCI Registration is required.Experience : 2+ years relevant experience in OBGY with 50+ beded multispeciality hospital is required.Salary : Rs.70,000/- to Rs.1,20,000/- (Subject to Qualification, Experience...

Position - Clinical Assistant - Gynecology Qualification - BAMS + MD/ MS OBGY/ DGO /CGO Experience - 0 - 5 year Location -Pune **Job Type**: Regular / Permanent **Salary**: ₹30,000.00 - ₹50,000.98 per month **Benefits**: - Health insurance - Life insurance Schedule: - Rotational shift Ability to commute/relocate: - Pune, Maharashtra: Reliably...

Qualification: BAMS + MS (OBGY)Location: PuneExperience: 2 Years to 3 Years

**Job Type - Fresher or Internship level** Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe. **Responsibilities**: **1. Assist in Protocol Development**: -...

**Job Overview**: **Clinical Associate Orthopedic**: **Pune**: - Job Location:Baner - Experience:1-2 years - Salary: 80K-1.10 Lac - Job Type:Full Time - Work Location: - No of vacancies:1 **Urgent Requirement** **Clinical Associate Orthopedic** **Qualification**: - MBBS MS/ D.ORTHO **Experience**-1 TO 2 YEARS **Salary** 80K TO 1.10 lac per...

**Job Type - Fresher or Internship level** Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe. **Responsibilities**: **1. Assist in Protocol Development**: -...

As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research. Key Responsibilities : Conduct site visits to monitor trial activities and ensure compliance...

As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research.Key Responsibilities:Conduct site visits to monitor trial activities and ensure compliance...

As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research.Key Responsibilities:Conduct site visits to monitor trial activities and ensure compliance...

Specific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...

Specific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...

Responsibilities for Clinical Research Associate - Recruit and enroll study participants - Input clinical research data into electronic data systems - Coordinate patient visits and procedures related to research - Act as resource for study participants by answering questions and explaining related procedures - Ensure the study site is compliance with all...

Specific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...

Specific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...

Creating and writing trial protocols, and presenting these to the steering committee. - Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial. - Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion. - Ordering, tracking, and managing IP...