Opening for the post of Associate @ PAREXEL INTERNATIONAL
Job Description
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. PAREXEL 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.
JOB DESCRIPTION
Job Title: Senior Associate
Department: PCMS
SBU: Commercialization
Location: India
Essential Function
The Associate/Senior associate role involves review of scientific literature/evidence, analysis and medical writing to support regulatory and reimbursement submissions
Relationships
Reports To Manager/Director
Key Accountabilities
- Review scientific evidence emerging from clinical efficacy and safety studies
- Develop, run and validate literature searches for efficacy and adverse event data
- Analyze evidence based on standard network meta-analysis techniques
- Development of evidence based reports on clinical efficacy and safety to support reimbursement and regulatory requirements
- Independently work on a range of scientific deliverables ranging from abstracts, to detailed reports following a clear, concise and scientific style with attention to detail on the depth of the scientific content
- Ensure deliverables meet Parexel quality or best practice standards in medical writing of accuracy, clarity and neatness
- Communicate project outcomes clearly and concisely both internally and externally to the clients with support from project managers
Skills
- Excellent interpersonal, verbal and written communication skills
- Client focused approach to work
- A flexible attitude with respect to work assignments and new learning
- Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
- Willingness to work in a matrix environment and to value the importance of teamwork.
- Strong writing skills in terms of clear, accurate and concise scientific content writing; demonstrated track record of quality publications, presentations, and research or prior experience in medical content writing.
- Prior experience in client interaction will be preferred
- Hands on knowledge of computers especially Microsoft Excel & Microsoft Word
Education
- Recognized Post graduate or PhD degree in Pharmacy/ life sciences
Language Skills
- Good verbal and written English Communication skills
Minimum Work Experience
- Preferably 1-2 years of experience with a Pharma- KPO/ Pharmaceutical company, fresher may apply
02 to 05 years
Salary: Not Disclosed by Recruiter
Industry: Pharma / Biotech / Clinical Research
Functional Area: Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology
Role Category:R&D
Role:Bio/Pharma Informatics-Associate/Scientist
Click here to apply
Job Description
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. PAREXEL 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.
JOB DESCRIPTION
Job Title: Senior Associate
Department: PCMS
SBU: Commercialization
Location: India
Essential Function
The Associate/Senior associate role involves review of scientific literature/evidence, analysis and medical writing to support regulatory and reimbursement submissions
Relationships
Reports To Manager/Director
Key Accountabilities
- Review scientific evidence emerging from clinical efficacy and safety studies
- Develop, run and validate literature searches for efficacy and adverse event data
- Analyze evidence based on standard network meta-analysis techniques
- Development of evidence based reports on clinical efficacy and safety to support reimbursement and regulatory requirements
- Independently work on a range of scientific deliverables ranging from abstracts, to detailed reports following a clear, concise and scientific style with attention to detail on the depth of the scientific content
- Ensure deliverables meet Parexel quality or best practice standards in medical writing of accuracy, clarity and neatness
- Communicate project outcomes clearly and concisely both internally and externally to the clients with support from project managers
Skills
- Excellent interpersonal, verbal and written communication skills
- Client focused approach to work
- A flexible attitude with respect to work assignments and new learning
- Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
- Willingness to work in a matrix environment and to value the importance of teamwork.
- Strong writing skills in terms of clear, accurate and concise scientific content writing; demonstrated track record of quality publications, presentations, and research or prior experience in medical content writing.
- Prior experience in client interaction will be preferred
- Hands on knowledge of computers especially Microsoft Excel & Microsoft Word
Education
- Recognized Post graduate or PhD degree in Pharmacy/ life sciences
Language Skills
- Good verbal and written English Communication skills
Minimum Work Experience
- Preferably 1-2 years of experience with a Pharma- KPO/ Pharmaceutical company, fresher may apply
02 to 05 years
Salary: Not Disclosed by Recruiter
Industry: Pharma / Biotech / Clinical Research
Functional Area: Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology
Role Category:R&D
Role:Bio/Pharma Informatics-Associate/Scientist
Click here to apply
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