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Attention Fresher Pharma/ Life Science Candidates- Register now for National Entrance Exam to get hired in reputed MNC’s: See full post for details or call now

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<span style="color: red;"><b>Attention Fresher Pharma/ Life Science Candidates</b></span></div>
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now for National Entrance Exam to get hired in reputed MNC’s:</b></span></div>
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<span style="color: red;"><b>Click on link - <a href="https://docs.google.com/forms/d/1krqKT6SpDg2k6CO2Y0QGM6BSWEbtQVLyLj2Ru97XhqY/viewform">https://docs.google.com/forms/d/1krqKT6SpDg2k6CO2Y0QGM6BSWEbtQVLyLj2Ru97XhqY/viewform</a></b></span>
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Attention Fresher Pharma/ Life Science Candidates- Register now for National Entrance Exam to get hired in reputed MNC’s: See full post for details or call now

Attention Fresher Pharma/ Life Science Candidates Register now for National Entrance Exam to get hired in reputed MNC’s: Click...

Opening of Accenture for Rmedical Reviewer- Bnagalore "H3"

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<table align="center" border="0" cellpadding="4" cellspacing="1" class="jobsTable" style="width: 100%px;"><tbody>
<tr><td class="detailJob">About Accenture Accenture is a global management consulting, technology services and outsourcing company, with more than 323,000 people serving clients in more than 120 countries. Combining unparalleled experience, comprehensive capabilities across all industries and business functions, and extensive research on the world's most successful companies, Accenture collaborates with clients to help them become high-performance businesses and governments. The company generated net revenues of US$30.0 billion for the fiscal year ended Aug. 31, 2014. Its home page is www.accenture.com.</td></tr>
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<tr valign="top"><td class="jdHead" width="20%">Designation</td><td class="detailJob" valign="top">Accenture is Hiring fo Rmedical Reviewer- Bnagalore</td></tr>
<tr valign="top"><td class="jdHead">Job Description</td><td class="detailJob" valign="top"><div style="background-color: white;">
Accenture is Hiring for rmedical reviewer- Bangalore</div>
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<u>Job Profile:</u></div>
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<li>1-4 yrs of relevent Experiece in Pharma covigillance& clinical practise</li>
<li>MBBS ,MCI Certified </li>
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<tr valign="top"><td class="jdHead">Desired Profile</td><td class="detailJob" valign="top">1-4 yrs of relevent Experiece in Pharma covigillance& clinical practise<br />
MBBS ,MCI Certified<br />
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Flexible to work  in shift timings<br />
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<tr valign="top"><td class="jdHead" width="20%">Experience</td><td class="detailJob" valign="top">1 - 6 Years</td></tr>
<tr valign="top"><td class="jdHead">Industry Type</td><td class="detailJob" valign="top">Medical / Healthcare / Hospitals</td></tr>
<tr valign="top"><td class="jdHead">Role</td><td class="detailJob" valign="top">Associate/Senior Associate -(NonTechnical)</td></tr>
<tr valign="top"><td class="jdHead">Functional Area</td><td class="detailJob" valign="top">ITES, BPO, KPO, LPO, Customer Service, Operations</td></tr>
<tr valign="top"><td class="jdHead" height="20">Education</td><td class="detailJob" height="20" valign="top"><em>UG - </em>MBBS - Medicine<br />
<em>PG - </em>M.S/M.D - Any Specialization<br />
<em>Doctorate - </em>Any Doctorate - Any Specialization, Doctorate Not Required</td></tr>
<tr valign="top"><td class="jdHead">Compensation:</td><td class="detailJob" valign="top"> Not disclosed</td></tr>
<tr valign="top"><td class="jdHead">Location</td><td class="detailJob" valign="top">Bengaluru/Bangalore</td></tr>
<tr valign="top"><td class="jdHead">Keywords</td><td class="detailJob" valign="top">pharma covigillance medical reviewew pv clinical practise pharmacovigilance practise pharmaceutical practise</td></tr>
<tr valign="top"><td class="jdHead">Contact</td><td class="detailJob" valign="top">Nithya </td></tr>
<tr valign="top"><td class="jdHead">Telephone</td><td class="detailJob" valign="top">08041063866</td></tr>
<tr valign="top"><td class="jdHead">Email</td><td class="detailJob" valign="top"><a href="mailto:" style="color: blue; text-decoration: none;">p.g.singh@accenture.com,shanthi.gopishwarrao@accenture.com</a></td></tr>
<tr valign="top"><td class="jdHead">Website</td><td class="detailJob" valign="top"><a href="http://www.careers.accenture.com/India" rel="nofollow" style="color: blue; text-decoration: none;" target="_blank">http://www.careers.accenture.com/India</a></td></tr>
<tr valign="top"><td class="jdHead">Job Posted</td><td class="detailJob" valign="top">2015-07-08 12:26:18.0</td></tr>
<tr valign="top"><td class="jdHead">Reference</td><td class="detailJob" valign="top">pharmacovigillance<br />
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Opening of Accenture for Rmedical Reviewer- Bnagalore "H3"

About Accenture Accenture is a global management consulting, technology services and outsourcing company, with more than 323,000 people se...

Opening for Clinical Research Associate inTechnosoft Global Services Pvt "H2"

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<span style="color: #333232; font-family: Arial, Helvetica, sans-serif; font-size: 14px; line-height: 20px; text-align: justify;">Technosoft Corporation is an IT and BPM services provider with its headquarter based in Southfield, MI, USA and 6 delivery centers across locations in India. We provide information technology, business process management and consulting services to companies in North America, Australia New Zealand and Asia-Pacific Regions. As a privately owned company we answer to only two constituencies – our clients  and our employees. Our clients rely on us to provide services and solutions that leverage our industry and domain expertise combined with our technology prowess, delivery focus and quality. Our collaborative culture and work environment helps attract and retain exceptional talent which is a key ingredient to address our clients needs and help drive our sustained growth. To see how Technosoft can go ‘Beyond Possible’ for your organizational needs, email us at </span><a href="mailto:wecanhelp@technosoftcorp.com" style="font-family: Arial, Helvetica, sans-serif; font-size: 14px; line-height: 20px; outline: none; text-align: justify; zoom: 0;" target="_blank">wecanhelp@technosoftcorp.com</a><span style="color: #333232; font-family: Arial, Helvetica, sans-serif; font-size: 14px; line-height: 20px; text-align: justify;">or visit us at </span><a href="http://www.technosoftcorp.com/" style="font-family: Arial, Helvetica, sans-serif; font-size: 14px; line-height: 20px; outline: none; text-align: justify; zoom: 0;" target="_blank">www.technosoftcorp.com</a><br />
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<span style="background-color: white; color: #296196; font-family: Roboto, sans-serif; font-size: 16px; line-height: 30px;">Job Description</span><br />
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Skill:Clinical data management, real world late phase, Clinical care options, Record Index Management.</div>
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Job location:Bangalore</div>
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Walkin Date:13th July 2015-17th July 2015</div>
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Time:9am to 5pm</div>
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Venue:Cessna Business Park</div>
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Embassy Tech Square,</div>
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Signet building west wing,</div>
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3rd floor,Kadubeesanahalli,</div>
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Marathalli</div>
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Landmark:New Horizon College</div>
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Contact Persons : Meena / Deepika</div>
<br style="margin: 0px; padding: 0px;" /><br style="margin: 0px; padding: 0px;" />Salary: Attractive<br style="margin: 0px; padding: 0px;" />Industry: Pharma / Biotech / Clinical Research<br style="margin: 0px; padding: 0px;" />Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology<br style="margin: 0px; padding: 0px;" />Role Category: Clinical Research Associate/Scientist<br style="margin: 0px; padding: 0px;" />Role: Clinical Research Associate/Scientist<br style="margin: 0px; padding: 0px;" />Keyskills: Clinical Research, Clinical Data Management, clinical data validation, pharmacovigilance, clinical programming</div>
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Desired Profile</div>
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<br style="margin: 0px; padding: 0px;" />Education:UG -Any Graduate, Graduation Not Required <br style="margin: 0px; padding: 0px;" />PG - Any Postgraduate, Post Graduation Not Required <br style="margin: 0px; padding: 0px;" />Doctorate - Any Doctorate - Any Specialization, Any Specialization, Doctorate Not Required</div>
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Opening for Clinical Research Associate inTechnosoft Global Services Pvt "H2"

Technosoft Corporation is an IT and BPM services provider with its headquarter based in Southfield, MI, USA and 6 delivery centers across l...

Pharmacovigilance / Drug Safety Specialist, Manager WDB Sigapore Pte. Ltd "H1"

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We, a Japanese CRO, are planning to establish the centre of Pharmacovigilance/Drug Safety.<br />We have some openings from specialists to managers in Pharmacovigilance.<br /><b style="unicode-bidi: embed;">Job Responsibilities:</b></div>
<ul>
<li>Receive, collect and track required data and enter into safety database.</li>
<li>Process data according to applicable regulations and guidelines, SOPs, and project requirements.</li>
<li>Triage and classify incoming events.</li>
<li>Write and amend existing company SOPs.</li>
<li>Prepare project KPI and monthly report.</li>
<li>Provide guidance and mentoring to less experienced/new staff members.</li>
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<b style="unicode-bidi: embed;">Job Requirements:</b></div>
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<b style="unicode-bidi: embed;">for Management role:</b></div>
<ul>
<li>Direct project management experience at a CRO or pharmaceutical company and Pharmacovigilance/Drug Safety experience.</li>
<li>Demonstrated supervisory skills.</li>
<li>Excellent interpersonal and presentation skills.</li>
<li>Demonstrated knowledge of pharmacovigilance regulatory requirements (i.e. Good Clinical Practice, ICH guidelines, etc.).</li>
</ul>
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<b style="unicode-bidi: embed;">for Specialist role:</b></div>
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<li>Thorough understanding of Good Clinical Practice (GCP),International Conference on Harmonisation (ICH) guidelines and global regulatory requirements.</li>
<li>In-depth knowledge of Pharmacovigilance/Drug Safety SOPs.</li>
</ul>
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<b style="unicode-bidi: embed;">Common requirements:</b></div>
<ul>
<li>Bachelor, MSc or equivalent in life sciences or a related field.</li>
<li>Ability to meet strict deadlines.</li>
<li>Presentation and report writing skills.</li>
<li>Demonstrate a positive and flexible working attitude.</li>
<li>Ability to establish and maintain effective working relationships with coworkers, managers and clients.</li>
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<b style="unicode-bidi: embed;">Notifications:</b></div>
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Interested candidates, please send your resume including:<br />a) Expected salary<br />b) Current and last drawn salaries<br />c) Availability<br />We regret only short listed candidate will be notified. All applications will be treated with the strictest confidence.<br />By submitting any application to us, it shall be deemed that you consent to our collecting, using, retaining and disclosing your personal information to prospective employers for their consideration.</div>
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Required experience:</div>
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<li>Pharmacovigilance: 1 year</li>
</ul>
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Pharmacovigilance / Drug Safety Specialist, Manager WDB Sigapore Pte. Ltd "H1"

We, a Japanese CRO, are planning to establish the centre of Pharmacovigilance/Drug Safety. We have some openings from specialists to manag...

Career opportunity as Medical Writer II in Parexel "H3"

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<span style="font-family: verdana, geneva, sans-serif; margin: 0px; padding: 0px;">PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.</span></div>
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<span style="font-family: verdana, geneva, sans-serif; margin: 0px; padding: 0px;"><span style="color: black; margin: 0px; padding: 0px;"><span style="color: indigo; margin: 0px; padding: 0px;"><b style="margin: 0px; padding: 0px;">Post: </b></span></span>Medical Writer II</span></div>
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<span style="font-family: verdana, geneva, sans-serif; margin: 0px; padding: 0px;"><span style="color: indigo; margin: 0px; padding: 0px;"><b style="margin: 0px; padding: 0px;">Job Description:</b></span><br style="margin: 0px; padding: 0px;" />Under departmental supervision, the Medical Writer II will research, create, edit, and coordinate the production of clinical documents associated with submissions to regulatory authorities including but not limited to: study protocols, model informed consents, interim and final clinical study reports and safety updates. The Medical Writer II will also be responsible for the production of clinical study documentation associated with clinical trials that may not be included in a regulatory submission. The Medical Writer II may serve as primary technical contact with client under appropriate departmental supervision.</span></div>
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<span style="font-family: verdana, geneva, sans-serif; margin: 0px; padding: 0px;"><b style="margin: 0px; padding: 0px;">Relationships</b><br style="margin: 0px; padding: 0px;" />Reports To Departmental Line Management, Medical Writing Services<br style="margin: 0px; padding: 0px;" />Directly Supervises None<br style="margin: 0px; padding: 0px;" />Provides Work Direction to Medical Writer I, Associate Medical Writer, Medical Writing Assistant<br style="margin: 0px; padding: 0px;" />Works Closely with Project Managers/Leaders Physicians, Biostatisticians, Data Managers, Regulatory Associates, Medical Writing staff<br style="margin: 0px; padding: 0px;" />External Relationships Client technical representatives</span></div>
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<span style="font-family: verdana, geneva, sans-serif; margin: 0px; padding: 0px;"><b style="margin: 0px; padding: 0px;">Key Accountabilities:</b><br style="margin: 0px; padding: 0px;" />- Write clinical documents associated with submissions to regulatory authorities including but not limited to: study protocols, model informed consents, interim and final clinical study reports and safety updates.<br style="margin: 0px; padding: 0px;" />- Serve as the primary client contact, negotiating deliverable timelines, and resolving project related issues, under departmental supervision. Project management of contractual and financial aspects may only be performed with the guidance of medical writing management.<br style="margin: 0px; padding: 0px;" />- Serve as the Medical Writing representative on assigned project teams, providing proactive support to Project Leadership for planning efficient work plans and timelines for medical writing deliverables, and medical writing input into other departmental deliverables. Identify any potential project challenges to departmental line management and project leader including changes in project plan, timeline or out of scope requests, and suggest possible resolution options.<br style="margin: 0px; padding: 0px;" />- Provide medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copyediting and content review.<br style="margin: 0px; padding: 0px;" />- Ensure document content and style adheres to FDA/EMA or other appropriate regulatory guidelines, and complies with departmental and corporate or client SOPs and style guidelines.<br style="margin: 0px; padding: 0px;" />- Coordinate and conduct interdepartmental team review and sign-off of document deliverables according to PAREXEL guidelines/SOPs including: distribute drafts, chair review meeting, incorporate revisions, document key project events, and complete sign-off procedures.<br style="margin: 0px; padding: 0px;" />- Coordinate production and distribution of draft and final documents to project team and client. Ensure that all work is complete and of high quality prior to team distribution or shipment to client.<br style="margin: 0px; padding: 0px;" />- Perform literature searches/reviews as necessary to obtain background information and training for development of documents.<br style="margin: 0px; padding: 0px;" />- Review statistical analysis plans and mock statistical output to determine the appropriateness of content/format for clinical writing.<br style="margin: 0px; padding: 0px;" />- Attend internal technical team and client team meetings as required.<br style="margin: 0px; padding: 0px;" />- May provide guidance to less experienced departmental members.<br style="margin: 0px; padding: 0px;" />- Supervise collection of materials by the Medical Writing Assistant or Associate Medical Writer for assembly of client deliverables and for filing appropriately in project files.<br style="margin: 0px; padding: 0px;" />- May participate in departmental or interdepartmental process improvement and training initiatives.<br style="margin: 0px; padding: 0px;" />- May participate in development of formats, templates and general guidelines for clinical documentation and workflow procedures. Assist in the development of departmental SOPs.<br style="margin: 0px; padding: 0px;" />- Keep abreast of professional information and technology through workshops and conferences, and ensure the appropriate transfer of that information to the department.</span></div>
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<span style="font-family: verdana, geneva, sans-serif; margin: 0px; padding: 0px;"><span style="color: indigo; margin: 0px; padding: 0px;"><b style="margin: 0px; padding: 0px;">Skills</b></span><br style="margin: 0px; padding: 0px;" />• Excellent interpersonal, verbal and written communication skills.<br style="margin: 0px; padding: 0px;" />• Client focused approach to work.<br style="margin: 0px; padding: 0px;" />• A flexible attitude with respect to work assignments and new learning.<br style="margin: 0px; padding: 0px;" />• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.<br style="margin: 0px; padding: 0px;" />• Willingness to work in a matrix environment and to value the importance of teamwork.<br style="margin: 0px; padding: 0px;" />• Demonstrated understanding of the drug development process.<br style="margin: 0px; padding: 0px;" />• Extensive clinical/scientific writing skills.<br style="margin: 0px; padding: 0px;" />• Advanced word processing skills/familiarity with Word for Windows.</span></div>
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<span style="font-family: verdana, geneva, sans-serif; margin: 0px; padding: 0px;"><b style="margin: 0px; padding: 0px;">Education</b><br style="margin: 0px; padding: 0px;" />• Bachelor's degree in Life Sciences/Health Related Sciences or equivalent.</span></div>
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<span style="font-family: verdana, geneva, sans-serif; margin: 0px; padding: 0px;"><b style="margin: 0px; padding: 0px;">Language Skills</b><br style="margin: 0px; padding: 0px;" />• Fluent in written and spoken English.</span></div>
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<span style="font-family: verdana, geneva, sans-serif; margin: 0px; padding: 0px;"><b style="margin: 0px; padding: 0px;">Minimum Work Experience</b><br style="margin: 0px; padding: 0px;" />• Medical writing experience: experience in writing multiple clinical study reports.</span></div>
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<span style="font-family: verdana, geneva, sans-serif; margin: 0px; padding: 0px;"><span style="color: indigo; margin: 0px; padding: 0px;"><b style="margin: 0px; padding: 0px;">Additional Information:</b></span><b style="margin: 0px; padding: 0px;"><br style="margin: 0px; padding: 0px;" /></b><b style="margin: 0px; padding: 0px;">Qualification:</b> <span style="margin: 0px; padding: 0px;">Bachelor's degree in Life Sciences</span><b style="margin: 0px; padding: 0px;"><br style="margin: 0px; padding: 0px;" />Location: </b>Karnataka - Bangalore<br style="margin: 0px; padding: 0px;" /><b style="margin: 0px; padding: 0px;">Industry Type: </b>Pharma/ Biotech/Clinical Research<br style="margin: 0px; padding: 0px;" /><b style="margin: 0px; padding: 0px;">Functional Area:</b> Medical Writing<br style="margin: 0px; padding: 0px;" /><span style="margin: 0px; padding: 0px;"><b style="margin: 0px; padding: 0px;">Requisition #:</b> pare-10043635</span><br style="margin: 0px; padding: 0px;" /><b style="margin: 0px; padding: 0px;">End Date:</b> 30<sup style="margin: 0px; padding: 0px;">th</sup> July, 2015</span></div>
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Career opportunity as Medical Writer II in Parexel "H3"

PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis....