Parexel hiring Associate Regulatory Affairs "A"

Associate Regulatory Affairs

1 - 2 YearsDelhi

Job Description

Experienced with preparation/review of Clinical Trial Application Packages for Asian countries including India.

Awareness of regulatory requirements

Review and evaluate technical and scientific data and reports required for submission

Monitor applicable regulatory requirements; assure compliance with the companys and external standards Co-ordinate with global team for documentation

Responding to queries raised by regulatory authorities

Maintain regulatory files in a format consistent with requirements

Label reviews

Tracking submissions

CTRI registration

Company Profile

PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Perceptive Informatics, Inc., a subsidiary of PAREXEL, provides advanced technology solutions, including medical imaging, to facilitate the clinical development process. Headquartered near Boston, Massachusetts, PAREXEL operates in approximately 70 locations throughout over 50 countries around the world, and has more than 13,000 employees. At PAREXEL, we have a passion for making a profound difference. As an expertise-based business, the caliber of our people and their dedication directly impacts our success, the success of our clients, and the ability to make a difference in the lives of patients worldwide. You'll be surrounded by supportive leadership and a brilliant team who share a common goal - to improve the lives of millions of patients.

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WALK IN INTERVIEW AT INDIAN INSTITUTE OF SOIL SCIENCES

CLICK HERE TO SEE DETAILS

http://www.careerbiotech.com/2016/09/walk-in-interview-at-indian-institute.html

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Regulatory Affiars Jobs "A"

Associate Regulatory Affiars

1 - 2 Years

Delhi

Job Description

Experienced with preparation/ review of Clinical Trial Application Packages for Asian countries including India.

Awareness of regulatory requirements

Review and evaluate technical and scientific data and reports required for submission

Monitor applicable regulatory requirements; assure compliance with the companys and external standards Co-ordinate with global team for documentation

Responding to queries raised by regulatory authorities

Maintain regulatory files in a format consistent with requirements

Label reviews

Tracking submissions

CTRI registrationCompany Profile

PAREXEL International Corporation is a leading global biopharmaceutical services organization, providing a broad range of expertise-based contract research, consulting, medical communications, and technology solutions and services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. PAREXEL Informatics provides advanced technology solutions, including medical imaging, to facilitate the clinical development process. Headquartered near Boston, Massachusetts, PAREXEL has offices nearly 80 locations in over 50 countries around the world, and has approximately 18,000 employees.

In India, PAREXEL has seven offices spread across five cities: Bengaluru, Hyderabad, Chandigarh, New Delhi and Mumbai. These offices are home to more than 3,000 employees.
Our two new offices in Bengaluru, called IndiQube and EcoWorld, were strategically designed to support a variety of work styles. There are collaboration zones in bright colors, freestanding high tables with stools to serve as informal meeting spaces, quiet rooms for group meetings, and private booths for phone calls. This innovative workspace encourages teamwork, and allows for sufficient flexibility to utilize the office beyond workstations.

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Walk in Interview- NATIONAL INSTITUTE OF MALARIA RESEARCH

NATIONAL INSTITUTE OF MALARIA RESEARCH 

(Indian Council of Medical Research) Sector – 8, Dwarka, New Delhi – 110077

Post 1: Project Manager- One Post – On consolidated salary of Rs.50,000/-p.m
Post 2: Office Assistant-one post(UR) On consolidated salary of Rs.17,040/- p.m
Post 3: Laboratory Attendant - Two posts (UR)- on consolidated salary of Rs.14,910/- p.m.

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Research Assistant Vacancy

Advertisement Notice Application is invited for the following post on project entitled “Neurological manifestations of Dengue fever: A Prospective study” sectioned by ICMR, New Delhi under the Principle Investigator Dr. Rajesh Verma, Professor Department of Neurology, KGMU UP, Lucknow. Name of the post : Research assistant Eligibility : M. Sc. Life Science & Two years experience Age : As per rule Salary : 27,000 per month (Fixed) Project duration: One year Application should reach the office of undersigned on/before 25 Aug 2016 at 04:00 pm along with the attested copies of certificate and testimonial. The interview will be held on 26th Aug 2016 at 11:00 am on the office of undersigned, Department of Neurology KGMU UP, Lucknow. No call letters for interview will be send separately. TA/DA will not be permissible for the appearing in interview. 

More Info :

https://kgmu.org/upload_file/user_download/9db5a0f6b3dfd1ba2e03809aacb7a700.pdf

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Lab Technicians / Scientific Officers

Lab Technicians / Scientific Officers - Cytogenetics

 Experience: 1 - 3 Years

Mumbai

Openings: 2

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Job Description

Qualification: B.Sc/ MSc DMLTExperience: 1 - 2 Years of experience preferably in Health Care Industry, Job Description: The Scientific Officer performs his duties diligently and methodically to analyse specimens allotted to him/ her. These specimens are analysed as per procedure for the test approved by the Director - Operations.The Scientific Officer is to perform those functions, which require subjective judgement to directly achieve analytical results, under supervision of the Lab Head.The Scientific Officer must receive approval of the Lab Head in making decisions in assessing calibration, control and acceptability of analytical runs for all laboratory data produced by themselves or other unlicensed personnel.The Scientific Officer must observe all laboratory safety precautions in the handling of clinical specimens and running of tests.The Scientific Officer must bring to the notice of his/ her section supervisor any abnormal findings/ test conditions required for specific attention of the supervisor.

Salary: Not Disclosed by Recruiter

Industry: Pharma / Biotech / Clinical Research

Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Role Category: Lab Technician/Medical Technician/Lab Staff

Role: Lab Technician/Medical Technician/Lab Staff

Desired Profile

Education:UG -B.Sc - Any Specialization
PG - M.Sc - Any Specialization
Doctorate - Doctorate Not Required

Company Profile

SRL is one of Worlds leading Clinical Diagnostic company

Advertisement: http://careers.srlworld.com/job-listings-Lab-Technicians-Scientific-Officers-Cytogenetics-SRL-Limited-Mumbai-Mumbai-Suburbs-1-to-3-years-110816001341

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