Product Manager job at Abbott

Product Manager job at Abbott

JOB DESCRIPTION:

Overall Job Purpose:

 Under general supervision, coordinate and provide technical marketing expertise for product promotions and marketing campaigns

 Support the design, development and implementation of marketing activities and materials

 Ensure the adherence of marketing activities and plans

 Coordinate involvement in conferences, exhibitions and marketing seminars

Roles and Responsibilities:

 Achieve Brand objectives, Sales and Division Margins to build enduring and profitable brands for Abbott

 Responsible for launching and managing Brands

 Responsible for managing strategic initiatives in listed therapeutic segments and meeting Key Opinion Leaders to understand the dynamics and the latest happenings in the therapy area

 Formulation and execution of the Marketing strategy for assigned Brands

 Cross-functional interaction with Finance, Supply Chain, Medical, Training to meet Brand objectives

 Responsible for providing the Sales Team with the necessary technical expertise to enable them to sell the product – this involves printed and electronic promotional material, product training, and relevant clinical papers

 Responsible for reviewing product data to ensure that the field force is kept up to date on new developments regarding the companies or competitors’ products

 Act as point of first reference for all product related enquiries and work collaboratively with colleagues to address any issues that may arise

 Close liaison with the field force to assess the response to and suitability of current promotional material and to ensure that the printed promotional material is being used optimally

 Liaise with the advertising agency regarding product campaigns

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Clinical Data Specialist Opening

Clinical Data Specialist Opening @ PRA

Overview

Provide timely and professional ongoing management of clinical trial data by identifying and resolving errors and inconsistencies in eCRF data to ensure consistently high standard database(s) with respect to cost, quality and timelines.

Responsibilities

Provide professional DM input on Clinical Trial Team(s)

Input to and review of clinical trial database design including User Acceptance Testing (UAT).

Provide input for the Validation and Analysis Plan (VAP) meeting for the clinical trial, which includes taking an active part in the meeting, providing input in writing the study specific validation checks and necessary reports to ensure high quality and consistent data.

Identify errors and inconsistencies; resolve them or initiate their resolution either via the field monitor or directly with the investigational site, to ensure high quality and timely database locks.

Review and contribute to preparation of protocols, specifically related to the data management section, visit schema and study design with supervision.

Prepare Case Report Forms (CRFs) and CRF completion Guidelines (CCGs), electronic or paper.

Support and assist data management staff for allocated trials.

Freeze and lock data as appropriate in time for statistical review, blinded interim quality review, interim and final database lock.

Perform training on data management software and practices or trial specific  topics as required.

May participate in preparation of training materials for data management activities and processes.

KPIs:

Meet established KPIs.  Timely and high quality completion of Data Management deliverables according to established objectives, including:  CRF Design, UAT of eCRF.  Fast and high quality Database Lock, EDC User Training.

Qualifications

Education (minimum/desirable):

University or college degree in life science, computer science, pharmacy, nursing or equivalent relevant degree.

Languages:

Fluent English (oral and written).

Experience/Professional requirement:

Minimum of 2 years experience in drug development and at least 1 year experience in Data Management

University Science Degree in life sciences, pharmacy, nursing or equivalent relevant experience.

Excellent written and oral English skills

Understanding of clinical trial methodology, GCP and medical terminology

Good computer skills

Good organizational and project management skills.

Good communication and interpersonal skills

Basic presentation and problem solving skills

Ability to work well in a team with or without supervision

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Quality Control Associate @ Accenture

Quality Control Associate @ Accenture

Job Location: Bangalore

Job Number: J4010

- Job description

OVERALL PURPOSE OF JOB

Train newly joined hires on Pharmacovigilance related work and also help in creating training documents.

Responsibilities/Authorities :

o    Conduct more complex job-training programs.

o    Develop and Conduct training programs for new and experienced resources in conjunction with training team and build an evaluation system to assess the trainees.

o    Provide feedback to trainees and the supervisors to ensure ongoing development of the trainee.

o    Required to learn Adverse event processing (AEP) & systems, to be an effective information source to new hires.

o    Identify additional training needs and assist in planning to address them.

o    Assure proper training documentation is maintained.

o    Assess effectiveness of training program and suggest change.

o    Maintain competency in areas being trained.

o    Teach, qualify, and mentor staff in the Trainer I role.

o    Provide assistance to Management team in improving the quality.

o    Provide regular updates on new tools and processes.

o    Responsible for generating reports regarding the trainees.

o    Assist HR in recruitment and selection process for new hires.

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Medical Coding Analyst jobs "A"

Accretive Health (NYSE: "AH") is a leading provider of services and technology to healthcare providers. Our mission is to help our healthcare clients strengthen their financial stability and deliver better care at a more affordable cost to the communities they serve, increasing healthcare access for all. Our distinctive operating model that includes people, process, and sophisticated integrated technology helps our customers realize sustainable improvements in their operating margins and improve the satisfaction of their patients, physicians, and staff. Our customers typically are multi-hospital systems, including faith-based or community healthcare systems, academic medical centers and independent ambulatory clinics, and their affiliated physician practice groups. Accretive Health offers a continuum of offerings to service our clients' needs. These offerings include: Provider Business Solutions ("PBS"), which improves the entire revenue cycle of our provider clients, unlike competing services that address only a portion of the revenue cycle or focus solely on cost reductions; Physician Advisory Services ("PAS"), which works closely with the hospital medical staff, case management, and senior leadership to strengthen compliance, limit denials, improve revenue integrity, and improve efficiency; and Population Health Solutions ("PHS"), which spans the entire healthcare delivery continuum and enables providers to manage the health of their patient populations by delivering higher-quality care while reducing aggregate cost of care.

Job Description

Review clinical documentation and diagnostic results as appropriate (i.e., to extract data and apply appropriate ICD-10-CM/CPT-4 codes for billing, internal and external reporting, research, and regulatory compliance). Under the direction of Health Information Management, must be able to accurately code conditions and procedures of at least one outpatient patient type (ED, ancillary, radiology, ePARS) per the Coding  Guidelines. Essential Duties and Responsibilities *Looking only for Same Day Surgery Coders( SDS) *5 to 7 activities and outcomes that require a significant amount of time and/or periodic tasks and outcomes that are critical to the job *Provide an indication of task or outcome complexity *Throughly reviews all documenation in the medical record and assigns codes for all diagnoses, treatments, and procedures according to the appropriate classification system for outpatient encounters. * Reviews physician assigned diagnosis code after thorough review of the medical record and, if necessary, queries physician for additional clarity in a professional manner. * Able to accurately abstract information from the medial records into the abstract system, according to established guidelines. * Abides by the Standards of Ethical Coding as set forth by the American Health Information Management Association (AHIMA) and adheres to official coding guidelines. * Consistently meets all productivity and quality metrics Typical Qualifications 1. CPC, CPC-H or CCS 2. Must be able to demonstrate proficiency in at least one outpatient coding type with 95%-99% accuracy. 3. 0-2 years of outpatient experience. 4. Must be able to use standard office equipment and information systems 5. Ability to interact with other employees through effective communication. 6. Ability to prioritize and shift workloads. Apply now

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Accenture hiring "A"

NH - Medical Reviewer

1 - 3 YearsChennai

Job Description

Position Purpose

The Associate Medical Director/ Medical Director (PSSR MD) performs the medical assessment activities related to drug safety pharmacovigilance for the assigned therapeutic area(s). The PSSR MD proactively evaluates safety information from individual cases and cumulative data, identifies and analyzes potential signals, and communicates data-driven conclusions to internal and external stakeholders.

Primary Responsibilities

Perform single case medical assessment, including the determination of seriousness, expectedness/ listedness/ labeledness, and causality of adverse events in compliance with current regulations, internal and external guidance documents, Standard Operating Procedures, Safety Job Aids, the Argus User Reference Guide and case processing/ coding conventions.

Maintain the timely submission of expedited reports.

Support the achievement of the Therapeutic Areas case processing performance timelines. Identify cases that meet SUSAR reporting criteria, prepare the SUSAR narrative, perform risk assessment, initiate the unblinding process (as appropriate), and make the report available for distribution.

Identify and evaluate safety signals based on individual cases and cumulative data assessment and by using other signal detection systems. Provide data-driven decisions and communicate these findings proactively and effectively to the key stakeholders.

Partner with Worldwide Safety Strategy and with other Worldwide Safety and Regulatory Safety Operations functional groups to monitor the safety profile of assigned products.

Actively participate in Risk Management Committees and other risk management activities for assigned therapeutic areas. Perform product safety reviews as appropriate.

Provide medical safety input as appropriate to Clinical Development Teams regarding expectedness/ listedness/ labeledness, causality, and data reconciliation

Company Profile

Accenture is a leading global professional services company, providing a broad range of services and solutions in strategy, consulting, digital, technology and operations. Combining unmatched experience and specialized skills across more than 40 industries and all business functionsunderpinned by the worlds largest delivery networkAccenture works at the intersection of business and technology to help clients improve their performance and create sustainable value for their stakeholders. With approximately 373,000 people serving clients in more than 120 countries, Accenture drives innovation to improve the way the world works and lives. Visit us at www.accenture.com

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Medical Writer jobs "A"

Hiring For Medical Writers for Mumbai Location

Adventures International Pvt Ltd

2 - 6 yrs

Mumbai

Job Description

*Draft Narratives
*Perform 100% data-review and finalization of Narratives
*Fill the defect tracker and track errors in every medical writing project
*Review and QC all deliverable

Interested Candidate drop your resume to ravali@adso.com

Company Profile:

Adventures International Pvt Ltd

SAP Services Partner and an advanced Information Technology consulting firm with over 15 years of industry experience. Since 1998, we have partnered with Fortune 500, mid-size and Public sectors to deliver valuable business solutions.  

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Novartis hiring "A"

 Business Process Controller

Novartis Healthcare Pvt. Ltd.

5 - 10 yrs

Hyderabad / Secunderabad

Job Description

Company: Novartis Healthcare Pvt Ltd
Position: Business Process Controller - Financial Control and Compliance
Job Location: Hyderabad
Qualification: Chartered Accountant

Position Purpose 
The BPC will be responsible for the creation, validation, quality control and distribution of de-fined compliance reports and financial data diagnostics and trend analyses for Countries, Regions and Global BPC, in the timelines, quality standards and consistency defined Group and Division Compliance processes.

Major Accountabilities 
Cross-divisional data analytics (PH, Alcon, AH, OTC) for compliance reviews 
- Pre-visit FC&CR data analytics 
- Compliance data analytics (such as Japan, South Africa & MENA) 
- Ad-hoc Data Analytics (such as NFCM analytics support for LCM / DCM & HRCF) Cross-divisional IA support 
- Monthly action item tracking - Monthly learnings from IA - Quarterly learnings deck 
- Quarterly learnings deck for HR (IA & BPCR) 
- Best practice sharing Cross-divisional FCCRs 
- Planning & execution 
- Monitoring completion and report issuance 
- Monitoring overdue action items 
- Learnings and best practice sharing (ad-hoc) 
- Tracker tool administrator Preparation of PH compliance decks 
- Monthly PFLT deck - Monthly FRALT deck - Quarterly BPCLT deck Others - Share point for cross-divisional FC&CR 
- Bi-monthly compliance cockpits

Minimum requirements
Chartered Accountant, with 5- 7 years exp in internal audit, financial control and compliance, Sox testing, Risk management.

Functional Experience:
5-7 Yrs experience in matrix multinational business environments 
Audit experience useful (internal). 
Sound knowledge of project management
Sound knowledge of financial controls & SOX requirements 
Professional relationship to external auditor
Application and understanding of the project management tool

Company Profile:

Novartis Healthcare Pvt. Ltd.

A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes us one of the most rewarding employers in our field.  

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Deloitte jobs "A"

Senior Analyst -quality Assurance- Hyderabad

Deloitte

2 - 7 yrs

Hyderabad / Secunderabad

Job Description

About DeloitteDeloitte is the brand under which tens of thousands of dedicated professionals in independent firms throughout the world collaborate to provide audit, consulting, financial advisory, risk management, and tax services to selected clients. These firms are members of Deloitte Touche Tohmatsu Limited (DTTL), a UK private company limited by guarantee. Each member firm provides services in a particular geographic area and is subject to the laws and professional regulations of the particular country or countries in which it operates. DTTL and each DTTL member firm are separate and distinct legal entities. Each DTTL member firm is structured differently in accordance with national laws, regulations, customary practice, and other factors and may secure the provision of professional services in their territories through subsidiaries, affiliates, and/ or other entities. In the United States, Deloitte LLP is the member firm of DTTL. Services are primarily provided by the subsidiaries of Deloitte LLP, including: Deloitte & Touche LLP Deloitte Consulting LLP Deloitte Financial Advisory Services LLP Deloitte Tax LLPIn India, Deloitte LLP has the following indirect subsidiaries: Deloitte & Touche Assurance & Enterprise Risk Services India Private Limited, Deloitte Consulting India Private Limited, Deloitte Financial Advisory Services India Private Limited, Deloitte Tax Services India Private Limited, and Deloitte Support Services India Private Limited. These entities primarily render services to their respective U. S. -based parents. U. S. India Support Services India Private LimitedDeloitte Support Services India Pvt Ltd. (U. S India Enabling Areas (EA)) at the U. S. India offices are the support arm of the organization and comprise several groups including Talent, Technology, Finance, Communications, Field Operations, etc. EA gives every client-service business unit access to the best and brightest resources when it comes to support services. More specifically, EA enables the business units to solely focus on satisfying clients and developing new products and services to sustain competitive advantage, while they consolidate and standardize a diverse collection of systems, processes, and functions. The team provides a wide array of services to the U. S firms and U. S India professionals, and is continually evaluating and expanding its portfolio. Global Digital Learning ServicesGlobal Digital Learning Services (GDLS) offers an entire array of learning and systems support to the Deloitte Learning Network, which includes Learning & Development professionals from all member firms across the globe. The GDLS team operates in India, Netherlands, United Kingdom, and United States. The GDLS team continuously aims to deliver innovative learning systems and solutions and also provides training administration services at the global, regional, and member-firm level to member firms, in order to enable learning administrators to provide a multitude of learning opportunities to their learners. Job descriptionFunction Deloitte Support Services India Pvt Ltd. Service line Global Digital Learning ServicesJob level Analyst - Career Level 3Specific skill set required Quality Assurance experience, copy editing, content writing, eLearning functionality and GUI testingGraduation Any Discipline 00Professional qualification Any Masters DegreeWork experience 4-6 years of related experience in eLearning or a journalistic capacityThe key job responsibilities include the following: Support quality assurance needs across all Deloitte Touch Tohmatsu Limited - Member Firms related learning materials Collaborate with Subject Matter Experts (SMEs) and clients and check learning modules Comprehend project scope and align quality checks with the given project scope Review print and electronic copy (including web content) for grammar, punctuation, readability, style, and flow Demonstrate excellent writing skills and oral communication skills while interacting with project managers, peers, and  all personnel Adhere to the project timelines. Any escalation or impact that can change the timeline should be brought to the managements attention as soon as possible Adhere to the quality assurance processes set by GDCS and ensure usability and functionality of learning content and identify any issues/ errors that could impact the learners experience Provide regular project updates to project managers Escalate any issues affecting timeliness or the scope of the design/ development project Create quality dashboards and identify training needs within the team Analyze quality assurance project requirements and work with project managers around scope and solution Ensure accuracy, completeness, and adherence to the established format in all deliverables Check training materials associated with the project including instructor guides, participant guides, hands-on activities, handouts, job aids, and self-study materials Demonstrate a strong understanding of language, ID theories, and the quality assurance process Work under pressure and deliver within tight timelines and be flexible to meet changing project demands and timelines Coordinate with the Instructional Design and Graphic Design teams Sign off quality deliverables with zero/ minimum errorsThe key skills required are as follows: Education: Masters degree in Journalism or English Literature from a recognized and reputed university Work Experience: At least 4-7 years of experience in quality assurance in learning/ corporate or journalism domain. Preferred: Experience in ID/ content development and/ or technical writing and copy editing Professional quality assurance/ editorial experience. This includes the ability to:o Review content for grammar, punctuation, readability, style, and content flow. o Research and analyze instructional materials for WBT(Web-based training)/ CBT(Computer-based training)/ ILT (Instructor-led training)o Do the quality assurance check for different types of input material o Use templates in doing the quality assurance check Knowledge of courseware development tools such as Storyline, Captivate, Prezi, Camtasia, Articulate Presenter, and Lectora would be an advantage. Strong organizational skills and attention to detail and ability to balance multiple tasks while working with a team to meet deadlinesOther Skills Keen attention to detail and accuracy Strong written communication skills (English) and listening and analytical skills Strong interpersonal traits including confidence, responsiveness, flexibility, initiative, decision making, conflict resolution, and tact Ability to work independently and as a team member Ability to interact with all levels of personnel and the ability to to direct questions appropriately Strong organizational skills, ability to prioritize, and multitask as needed Ability to adapt to a changing environment and approach challenges with creativity, resourcefulness in problem solving. Ability to work with confidential information Proficient with MS Office, specifically MS Word and PowerPointOther detailsWork timing 11:00 AM to 8:00 PM and 2:00 PM to 11:00 PM (expected to stretch during peak periods)Location Hyderabad 1Disclaimer: Please note that this job description is subject to change based on the business/ project requirements and at the discretion of management. Company Profile:

Deloitte

Deloitte is the brand under which tens of thousands of dedicated professionals in independent firms throughout the world collaborate to provide audit, consulting, financial advisory, risk management, and tax services to selected clients. These firms are members of Deloitte Touche Tohmatsu Limited (DTTL), a UK private company limited by guarantee. Each member firm provides services in a particular geographic area and is subject to the laws and professional regulations of the particular country or countries in which it operates. DTTL does not itself provide services to clients. DTTL and each DTTL member firm are separate and distinct legal entities, which cannot obligate each other. DTTL and each DTTL member firm are liable only for their own acts or omissions and not those of each other. Each DTTL member firm is structured differently in accordance with national laws, regulations, customary practice, and other factors, and may secure the provision of professional services in its territory through subsidiaries, affiliates and/or other entities.

In the United States, Deloitte LLP is the member firm of DTTL. Like DTTL, Deloitte LLP does not provide services to clients. Instead, services are primarily provided by the subsidiaries of Deloitte LLP, including:

Deloitte & Touche LLP

Deloitte Consulting LLP

Deloitte Financial Advisory Services LLP

Deloitte Tax LLP  

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Teaching Faculty required "A"

Teaching Assistant - Dairy Microbiology

Kerala Veterinary and Animal Sciences University (KVASU)

Thiruvanthapuram

Job Description

Note: Teaching Assistant engaged on daily wage basis will not have any preferential claim in the University service other than the right to receive remuneration of Rs.1200/- per day, subject to a monthly ceiling of Rs.30,000/- (Rupees Thirty Thousand only) for Professional Post Graduates and Rs.1000/- per day, subject to a monthly ceiling of Rs.25,000/- (Rupees Twenty Five Thousand only) for Post Graduates in other disciplines and Professional Graduates. This engagement is purely provisional and it will be terminated on short notice or when a regular hand / employment hand (those recruited through employment exchange) joins duty whichever is earlier.


Qualification: M. Tech./M.Sc. in Dairy Microbiology 

In the absence of candidates with above qualification, those with B. Tech (Dairy Science & Technology) shall be considered


A walk in interview for engagement of qualified persons for the following posts purely on daily wage basis in various teaching departments of the College of Dairy Science and Technology, Chettachal, Thiruvananthapuram is scheduled to be conducted on 05/07/2016 (Tuesday) from 10:30 A.M. onwards at the College Office, KELTRON Equipment Complex (2nd Floor), Karakulam Thiruvananthapuram. Candidates possessing requisite qualifications shall report at the venue with the originals of all certificates and testimonials to prove age, qualifications & experience. They are also advised to bring one set photocopies of their certificates/documents. No T.A. /D.A. will be paid to the candidates appearing for the interview.
Company Profile:

Kerala Veterinary and Animal Sciences University (KVASU)

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Syngene, Bangalore hiring "A"

Associate Scientist, PCO Toxicology

0 - 5 YearsBengaluru/Bangalore 

Job Description

Principal Accountabilities/ Responsibilities (Describe in bullet points, the duties and tasks of this position)

-The candidate must possess a strong background and experience in the theory and practice of discovery pathology -Ability to conduct necropsies and recognize, describe and interpret findings at necropsy -Strong background in animal models of diseases and experience in evaluating tissues from discovery biology studies including immunotechniques -Ability to evaluate tissue sections from discovery toxicity studies, including the interpretation of microscopical findings is preferable -Excellent verbal and written communication skills -Excellent interpersonal and teamwork skills

Skills :

The candidate should be having the expertise in multiple areas within the industrial pathology and drug discovery biology domains. Pathology- Should have basic understanding of principles involved in characterizing the pathology of efficacy models. Ability to read and understand the published literature of the respective animal models and applying the concepts to characterize them in house. Should have experience as a study pathologist in preclinical efficacy studies, data analysis, interpretation, preparation of reports and communication of findings with perspective to the cross functional teams. Should have a thorough knowledge in comparative anatomy, histology and histopathology. Should have directed a pathology lab with good understanding of the procedures such as necropsy and descriptive gross pathology. Good collaboration with various cross functional stakeholders, excellent communication skills and core behaviors should be must.

Key behaviors to be demonstrated for success in the role :

Innovation, team work and quick learner

Interfaces and Dependencies (Describe briefly the functions and people with whom the job-holder in this position will need to interact and coordinate with)

Company Profile

Incorporated in the year 1994, Syngene International is one of India's premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities. The state-of-the-art research facilities have been qualified by various pharmaceutical majors & regulatory agencies and has received various certifications including ISO 9001: 2008, ISO 14001:2004, OHSAS 18001:2007, GLP and AAALAC.

Over the past 16 years, Syngene has successfully partnered with leading pharmaceutical companies, large biotech companies, crop protection companies and cosmetics companies. Syngene together with  Bristol-Myers Squibb has set up a dedicated research facility in Bangalore to help advance Bristol-Myers Squibb's work in discovery and early drug development.

To advance its programs and expand its capabilities, Syngene is looking to recruit outstanding scientific talents.

So come and join us in our journey of scientific innovation.

For further details, please visit www.syngeneintl.com.

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Walk-in Interview on 29th June "A"

Walk-in at Thomson Reuters for Research Analyst on 29th June 2016

Thomson Reuters India Pvt Ltd

2 - 4 yrs

Hyderabad / Secunderabad

Job Description

Thomson Reuters Hiring For Research Analyst For IP & Science 

Job Description 

Participates in an Editorial or Content Operations team and assists in the creation and/or acquisition, preparation and delivery of assigned content and information for creating products and product functionality in all publication media (print or electronic). The primary focus at this entry level is training with some supervision. Conducts detailed, comprehensive searches and creates in-depth analysis on assigned research
projects.
Researches and extracts data from all applicable sources, ensures accuracy and quality of findings
by complying with policies and applicable laws.
Develop appropriate search queries to maximize research results.
Provides regular communication and feedback to client. Provides regular status updates on research
projects to manager.
Effectively manage workload within defined deadlines and budgets.

Qualification : MSc Biotechnology, Biochemistry, Microbiology, Genetics in Pharma or life sciences domains. MPharm- Pharmacology with 2-4 years experience in KPO industry with knowledge on patents and literature content .Phd in Life Science discipline with pharmacology knowledge

Experience : 2- 4 Years 

Walk -in Date & Venue : Hyderabad

Job location: Thomson Reuters, Plot no 14, Solitaire Building, Madhapur, Hyd
Land Mark: Near to INORBIT Mall.
Walk-in date: June 29th 2016 (Wednesday )
Walk-in time: 9:00 AM - 9:30 AM
Contact Person : Vijay Prakash

Please carry a Pen and a print out of this mail.

Company Profile:

Thomson Reuters India Pvt Ltd

Thomson Reuters is the world's leading source of intelligent information for businesses and professionals. We combine industry expertise with innovative technology to deliver critical information to leading decision makers in the financial, legal, tax and accounting, scientific, healthcare and media markets, powered by the world's most trusted news organization. With headquarters in New York and major operations in London and Eagan, Minnesota, Thomson Reuters employs more than 50,000 people in 93 countries. More information about Thomson Reuters and its financial performance can be found on www.ThomsonReuters.com.  

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Biotechnology Jobs "A"

 Research Analyst ( Biotechnology, MBA)

KuicK Research

0 - 2 yrs

Delhi

Job Description

* Internet Research/ Desk Research/ Secondary research.
* Content Writing & Content Development.
* Write market/Industry research studies.
* Find information on internet pertaining to companies.
* Analyze and classify the information collected.
* Organize the information / analysis in the desired output formats.
* Track news / developments related to targeted Industry, Company.
* Synthesize data out of multiple data sources to perform analysis about industry/companies.
* Business & Market Intelligence.
* Client Engagement.


How to Apply:


Interested eligible candidates need to write up an article on one of the below topics for 1200-1500 words. And send it along with your resume to avinash@kuickresearch.com


NOTE: RESUME WITHOUT THE ARTICLE WILL NOT BE CONSIDERED.


Article topics:
* Global Biosimilar Market
* Global Cancer Immunotherapy Market
* Global Cancer Vaccine Market
* India Power Transmission & Distribution Sector
* USA Shale Gas Sector
* Saudi Arabia Mutual Fund Industry
* India Logistics Industry

Company Profile:

KuicK Research

Kuick Research is not just another market research firm. We partner with our customers to provide research and consulting reports in areas appropriate to our customers' requirements. Our syndicated research team works acts as a knowledge partner for our customers so that we can provide detailed reports in areas that are relevant for our customers. Our team of highly trained syndicated research analysts creates reports which provide you with broad technical and market trends.  

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