Cognizant hiring for Clinical Data Management "A"

 Job Description:





End to End CDM activities
Relevant experience in Clinical Data Management
Perform data management activities on the assigned project in a timely and efficient manner
Generate queries to clarify and improve the quality of the data
Test and execute validation procedures


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Sun Pharma Hiring For the Post Of Clinical Research Associate "A"

Job Description :

• Facilitate and coordinate with investigator and site for EC submission and approval.
• Conduct site feasibility and qualification visits.
• Get trained on trial and documents.
• Prepare for kickoff
• meetings to train vendor representatives involved if outsourced
  activity for monitoring.
• Coordinate with investigator and sites for IM and assist PM in planning for IM
• Conduct SIVs, write SIV reports, and dispatch to sites
• Resolve queries and problems at sites and with vendors.

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Walk in for Clinical Data Management for Mumbai "A"

Job Description

Hi!!


We have a Walk in drive for Clinical Data Management for Mumbai location.


Qualification: Graduate/Post Graduate in Science/Life Sciences/B.Pharm/M.Pharm


Experience : 2 to 4 years in Clinical Data Management.


Location: Powai - Mumbai


Walk in Drive: Saturday 8th Oct 2016


Time: 9.30 AM to 11AM

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Genpact hiring Regulatory Associate "A"

Job Description

Job Location: Mumbai
Job Position: Associate
Department: Regulatory Services
Work experience: Freshers
Regulatory activities such as:
Domain expertise in Regulatory Affairs.
IT literate in Microsoft office, in particular Excel, and a basic knowledge of how databases work
Tenacity and the willingness to develop new skills and be adaptive
Maintain knowledge of domestic and international legislation by continuous learning
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Walk in for Clinical Data Management for Mumbai "A"

Job Description

Hi!!


We have a Walk in drive for Clinical Data Management for Mumbai location.


Qualification: Graduate/Post Graduate in Science/Life Sciences/B.Pharm/M.Pharm


Experience : 2 to 4 years in Clinical Data Management.


Location: Powai - Mumbai


Walk in Drive: Saturday 8th Oct 2016


Time: 9.30 AM to 11AM



Job Description:


End to End CDM activities
Relevant experience in Clinical Data Management
Perform data management activities on the assigned project in a timely and efficient manner
Generate queries to clarify and improve the quality of the data
Test and execute validation procedures


Apply here

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Walk in Interview for SAS Programmer at Quintiles "A"

RESPONSIBILITIES


• Serve as Lead Programmer on the corporate team.
• Plan and coordinate database design, development, implementation, maintenance, and user support of clinical systems.
• Provide technical expertise in conjunction with internal and external clients.
• Program, test, and document databases in accordance with programming standards and validation procedures.
• Program database manipulation and transfers of data for internal and external clients.
• Mentor other team members and Lead Programmers in training and developing technical and/or database expertise.
• Independently bring project solutions to the CDP teams and the Clinical Data Programming department.
• May assist IT in developing and implementing new technologies.
• May assist IT in testing and evaluating new upgrades to technologies.
• May assist in developing, revising, and maintaining core operating procedures and working instructions.
• Meet objectives as assigned, and interact with the project team to organize timelines, responsibilities and deliverables.
• Develop and maintain good communications and working relationships with teams and external clients.

E-mail : Naveen.alexandar@quintiles.com

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Work as Principal Scientist in Zoetis | M.Pharm / Ph.D "A"

Responsibilities  
The incumbent will be responsible for leading a team of scientists engaged in conducting formulation research and development activities on generic molecules, reformulation of existing drug products for life cycle management and new chemical entities. The area of formulation research includes solid and liquid dosage forms for oral, topical and parenteral administration to animals. The scope of research activities would typically include pre-formulation, prototype formulation and scale up studies as part of product development and subsequently the transfer of processes and technologies to commercial manufacturing sites. The position will involve developing and executing technical plans to meet target drug product profiles through in house research as well as external collaborations. The incumbent will be expected to ensure effective collaboration with various stake holders and customer groups such as global development team, regulatory, quality, manufacturing, marketing and clinical organizations for successful and timely delivery of clinical supplies and manufacturing process transfers. Other than the research activities the candidate will also be responsible for maintaining and delivering required documentation such as protocols, reports, SOPs, CMC technical sections for regulatory submission etc. Effective communication skills, leadership skills and people development skills are essential. The position would involve managing direct reports and travel up to about 25% of time.




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Freshers Job : Start Your Research Career @ Reliance "A"

The Reliance Group is India’s largest private sector enterprise, with businesses in the energy and materials value chain. Group’s annual revenues are in excess of US$ 73bn. The flagship company, Reliance Industries Limited, is a Fortune Global 114 company and is the largest private sector company in India. Backward vertical integration has been the cornerstone of the evolution and growth of Reliance.


ob Accountabilities :

• To generate scientific/technical data  , using established systems, procedures and protocols
• Develop new systems and methods and tools
• May have responsibility for providing other individuals with instructions and guidance to complete tasks which have been assigned
• Performs part of a key activity using fairly routine activities within a specified work program varying the approach taken as the precise nature of the work output varies
• Working independently carry out work to required standards to a plan agreed with supervisor and using known and novel procedures
• Apply knowledge and experience to recognise problems and work with supervisor in finding solutions; advise supervisor of any backlogs and on likely timescales
• Using basic, established, local methods and techniques, find information for advising or discussing with supervisor

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Sun Pharma hiring for Sr. Manager Clinical Research "A"

Job Description

• Act as a medical resource to the company as a whole and particularly to the clinical research department (protocol, CSR writing/ review, adverse events, discussions with investigators, internal meetings). 
• To have responsibility for nominated therapeutic areas and assume overall management of the clinical trials within these areas 
• To be recognized as a company expert in the nominated therapeutic areas and provide input into in product development teams. 
• Represent the company via presentations to groups of experts, societies, regulatory bodies and at international meetings. 
• Write clinical development plans, develop budgets, & provide drug development inputs 
• Establish ongoing liaison with key opinion leaders and to ensure that significant developments in the field are identified and monitored. 
• Provide medical expertise in the review of adverse experiences and discuss patient management issues with investigators. 
• Attend and contribute to interdisciplinary team meetings relating to clinical investigational drug trials 
• Effectively collaborate with colleagues in related project team departments such as Regulatory, Quality Assurance, anufacturing, Bioanalytical , PK/PD, Discovery, and Marketing 

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Microbiologists Post Vacant @ Bisleri "A"

Exclusive Job : Microbiologists Post Vacant @ Bisleri

Job Description

Water Quality Checking
Monitoring Of Water treatment Plant
Housekeeping and Hygiene of Plant
Analysis of Customer Complaints
Organise Fumigation of Plant and Laboratory
Monitoring Pest Control of Plant
Calibration of All equipments in Plants

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Cognizant hiring for CLINICAL DATA MANAGEMENT "A"

Opening for Clinical Data Management for Mumbai

Job Description:

End to End CDM activities
Relevant experience in Clinical Data Management
Perform data management activities on the assigned project in a timely and efficient manner
Generate queries to clarify and improve the quality of the data
Test and execute validation procedures


**Candidate should be open for rotational shifts.


Apply now

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Work as a Team Member in Food Tech Division @ Aditya Birla Science & Tech Company "A"

Work as a Team Member in Food Tech Division @ Aditya Birla Science & Tech Company



Aditya Birla Science and Technology Company Private Limited (ABSTCPL) is the corporate research and development centre for the Aditya Birla Group. Located in Taloja, just outside of Mumbai in India, ABSTCPL supports the broad diversity of the Group’s businesses through multi-disciplinary teams of expert scientists and engineers who lead fundamental and applied research projects. The company aims to be a world-class organisation that delivers innovative solutions, continuously improves core competencies and executes effectively. The centre is supported by state-of-the-art equipment set in a one-of-a-kind brand new technology-led environment.
Following post is vacant and applications are invited for the same:
Name of the post: Team Member (Food Technology)
Job Number: 160106KX
Schedule: Full-time
Job Location: Mumbai, Maharashtra
Job Description:
To spearhead R&D programs and develop technology based new business opportunities especially in the Food & Ingredient synthesis Sciences & Technology related areas
Major Challenges:

• Responsibility of conceptualization, Defining Scope of Research and timely execution of R&D projects in the area of Food sciences
• Managing the technical team at ABSTCPL and regular interactions with different businesses
• Ensuring adherence to Project Management Tools and other systems of patents / publications, by self and the team during project execution
• Keeping abreast of latest technology in the areas related to Food, and Chemicals, Carbon Black of ABG.

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Openings @ Mondelez India for Scientist Position "A"

Openings @ Mondelez India for Scientist Position

Mondelēz India Foods Ltd is a leading global confectionery & snacks company. It began its operations in 1948 by importing chocolates. After 60+ years of existence, it today has six company-owned manufacturing facilities at Thane, Induri (Pune), Malanpur (Gwalior), Sricity (Andhra Pradesh), Baddi (Himachal Pradesh), and Hyderabad and 4 sales offices in New Delhi, Mumbai, Kolkata and Chennai. The corporate office is in Mumbai.
It operates in five categories in India viz., chocolate, confectionery, beverages, biscuits, gum and candy and markets 11 power brands which include Bournvita, Dairy Milk, Halls, Gems, 5Star, Choclairs, Perk, Celebrations, Bournville, Tang & Oreo. Mondelez India Foods Ltd dominates the chocolate market in India with approximately 70% share of the market.

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Quintiles hiring Trainee Clinical Data Coordinator "A"

Trainee Clinical Data Coordinator

Quintiles

0 - 0 yrs

Mumbai

Job Description

Hi All,


We have openings for Clinical Data Management Fresher Role.


Job Location:Thane (Mumbai)




Education Qualification: Bpharm /Mpharm /Msc.Biotechnology / Btech Biotechnology freshers are eligible to apply.

Company Profile:

Quintiles

Quintiles is the world's largest provider of biopharmaceutical development and commercial outsourcing services. We bring a fully integrated approach to build biopharma and life sciences solutions - from pipeline through portfolio to population health â„¢. A career with Quintiles connects you to great opportunity to achieve professional success and impact healthcare around the world.  

Apply here

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Quintiles hiring Medical Surveillance Specialist "A"

Medical Surveillance Specialist - Quintiles

Quintiles

2 - 6 yrs

Bengaluru/Bangalore , Mumbai

Job Description

Monitors, evaluates and analyzes laboratory results on a daily basis, from sponsor central laboratory. Laboratory safety parameters are monitored for each patient at every site throughout clinical drug trial

Conducts preliminary review of laboratory results relative to established protocol-specific reference range guidelines, using relevant clinical laboratory experience.

Maintains up-to-date laboratory knowledge via continuing education activities (i.e., completion of continuing education class, applicable QU courses, review of journal articles) or attendance at medical seminars

To participate in various Pharmacovigilance procedures including the processing of Adverse Event (AE) reports through tracking, data entry, quality control, report generation and submission, records management, as well as other project related and system support tasks

Based on clinical laboratory experience, identifies potentially significant trends or shifts in laboratory results and alerts Sponsor physicians

To perform CEVA (Clinical Event Validation and Adjudication) project tasks in the areas of endpoint adjudication committee coordination, core laboratory coordination, DSMB administration, and Steering Committee administration

Assist with Safety Reviews of Case Report Forms and Adverse Event and medical coding as requested

Company Profile:

Quintiles

Quintiles is the world's largest provider of biopharmaceutical development and commercial outsourcing services. We bring a fully integrated approach to build biopharma and life sciences solutions - from pipeline through portfolio to population health â„¢. A career with Quintiles connects you to great opportunity to achieve professional success and impact healthcare around the world.  

Apply here

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Fortis hospital is hiring Clinical Dietitian & Nutritionist "A"

Clinical Dietitian & Nutritionist Required at Fortis Vashi

0 - 5 Years

Navi Mumbai Openings: 1

Job Description

To plan and document balanced, nutritious and healthy meals for all indoor patients as per their medical requirements
To motivate and involve patients in the planning of diet for better acceptability
To take detailed rounds of different wards in order to plan diet individually as per patient condition.
To evaluate dietary intake of patients and do required nutrient analysis for doctors reference.
To organize diet counseling of the indoor patients and their attendants for healthy eating on the basis of their medical background.
To coordinate with the doctors for patients diet
To prepare diet charts of walk ins, follow-ups, referral cases and executives in OPD.
To do constant follow up with the nurses for patients diet.
To co-ordinate with the F&B department to ensure that meals served to the patients are according to their profile.
To Supervise major meal services of patients
To plan the composition and schedule of the enteral feed for critical patients in compliance with the physician specifications.
To taste patients meals and suggest modifications if required before service.
To maintain logbook for interdepartmental communication
Any other task assigned by the HOD and the management

Company Profile

Fortis Healthcare Limited is committed to clinical excellence and patient-centric healthcare, which is manifest in hospital design, patient services, medical programmes and the compassionate approach of medical and non-medical hospital staff. Fortis commissioned its first hospital in 2001 at Mohali, near Chandigarh, and has expanded its operations to become a network with an over 10,000 bed capacity across 68 hospitals

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Quintiles hiring for CRA "A"

 JOB! Openings at Quintiles - In House CRA Role

Quintiles

2 - 4 yrs

Thane

Job Description

Dear  All,


We are pleased to let you know that we have multiple openings for experienced Clinical Research Professionals for In House CRA (Remote/Risk Based Monitoring) role.


Skill Sets/Knowledge Required - Clinical Research, CRA, CRC, Risk Based Monitoring, Remote Monitoring, ICH - GCP, Clinical Trials


Overall and Relevant Experience - 2 to 3.5 years 


Job Location - Thane (Mumbai)


Interested Candidates kindly send your CVs on Goldy.Sachdev@quintiles.com


Job Description


PURPOSE
Provide project related assistance for assigned complex project(s), sites and project teams. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics.

RESPONSIBILITIES
Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines
Establish and maintain effective project/ site communications
Create and maintain relevant project documents
Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information
Participate in document management (creation, review, maintenance, storage, as applicable)

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Good knowledge of applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws,
regulations and guidelines
Strong written and verbal communication skills including good command of English language
Results and detail-oriented approach to work delivery and output
Good problem solving skills
Good planning, time management and prioritization skills
Attention to detail and accuracy in work
Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel
and PowerPoint
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Proven ability to work on multiple projects balancing competing priorities
Ability to coach/ mentor junior colleagues

MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelor's degree in life sciences/pharma or related field and min 2 years relevant experience; or equivalent combination of education, training and experience

PHYSICAL REQUIREMENTS
Extensive use of keyboard requiring repetitive motion of fingers.
Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
Regular sitting for extended periods of time.
May require working in shifts.

Company Profile:

Quintiles

Quintiles is the world's largest provider of biopharmaceutical development and commercial outsourcing services. We bring a fully integrated approach to build biopharma and life sciences solutions - from pipeline through portfolio to population health â„¢. A career with Quintiles connects you to great opportunity to achieve professional success and impact healthcare around the world.  

Apply now

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Clinical Research Associate required for Sitec Labs "A"

Clinical Research Associate.

Sitec Labs Private Limited

0 - 1 yrs

Navi Mumbai

Job Description

Medical writing, Preparation of protocol, case record forms, informed consent forms etc. Preparation of study summary, submission of proposal to IEC / IRB, preparation of clinical study reports. AE documentation,summation of reports and review.

Company Profile:

Sitec Labs Private Limited

Sitec Labs Pvt. Ltd., an ISO 9001:2008 Contract Research Organization (CRO).  

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Hiring for B.pharm Research Analyst "A"

WNS Hiring for B.pharm Research Analyst - Meet HR Pooja 02240112935

0 - 5 Years

Mumbai

Job Description

Greeting from WNS!!

WNS Hiring for Pharma Research Analyst

Walkin from 31st Aug - 2nd Sep 
Contact HR Pooja 02240112935.

Job description and key accountabilities:

Research and analyze business impacting and time sensitive business information in the Biopharmaceutical Industry.
BioPharmaceutical Databases Development through Business Research, Information analysis and profiling in given format for:
1. Drug database:
Researching through various company websites and collecting the details (such as molecule, chemical structure & properties, mechanism of action, therapeutic area, clinical phases etc) of marketed drugs and drugs under developmental pipelines

2. Life science conference Database:
Searching and capturing details on upcoming biopharmaceutical/ Life science conferences. Details about the location, conference title, speakers, sponsors, exhibitors or media involved are captured

3. Active Intel:
Researching & tagging the Biopharmaceutical Industry news/articles to the database

4. Clinical Trials:
Understanding & tagging the Conditions, Interventions & Sponsors to the Clinical Trial Database
.
5. Pharmaceutical Licensing agreements:
Capturing the details of pharmaceutical licensing transactions from company websites or Securities and Exchange Commission (SEC) files, annual reports etc

6. Ad Hoc Tasks:
Working on any Ad Hoc, short duration assignments/projects assigned by clients related to Biopharmaceutical Industry.


B.Pharma Grad
Minimum work experience: 0

Candidate Boundary Limits: Churchgate / CST till Mira Road, Kharghar and Kalyan
Drop / Pick Up Points: Dadar / Borivli / Vashi / Thane.

Special skills:
Excellent Communication Skills
Keen Interest in Secondary Research
Ability to interpret data and aid in arriving at the key findings
Decision making and judgment
Proficient in MS Office

Shift Timings: Rotations Shifts (7am 2.30pm, 2.30pm 10pm )

Interview Venue:
WNS Global Services,Plant 5, Gate NO 2, Godrej Compound,LBS Marg, Vikhroli West. Near Caf Coffee Day. Landmark: Caf Coffee Day.

Contact Person: Miss Pooja.P

Synopsis about WNS:
WNS is a leading global KPO and BPO company. WNS has a strong horizontal focus with its Finance & Accounting, Contact Center and Research & Analytics solutions. WNS 'extends the enterprise' of some of the world's best brands by providing vertical-led solutions for Travel & Leisure, Banking & Financial services, Insurance, Shipping & Logistics, Utilities, Healthcare, Manufacturing, Telecommunications, and Retail & Consumer Packaged Goods industries.
 Company Profile

WNS is a leading global KPO and BPO company. WNS has a strong horizontal focus with its Finance & Accounting, Contact Center and Research & Analytics solutions. WNS 'extends the enterprise' of some of the world's best brands by providing vertical-led solutions for Travel & Leisure, Banking & Financial services, Insurance, Shipping & Logistics, Utilities, Healthcare, Manufacturing, Telecommunications, and Retail & Consumer Packaged Goods industries

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Jobs in Clinical Data Management @ Cognizant "A"

Opening for Clinical Data Management for Mumbai and Kolkata

4 - 9 Years

Job Description

Hi!!


We have an urgent opening for Clinical Data Management for Mumbai and Kolkata location.


Qualification: Graduate/Post Grraduate in Science/Life Sciences/B.Pharm/M.Pharm


Experience : 4years+  in Clinical Data Management.


Job Description:


End to End CDM activities
Relevant experience in Clinical Data Management
Perform data management activities on the assigned project in a timely and efficient manner
Generate queries to clarify and improve the quality of the data
Test and execute validation procedures



**Candidate should be open for rotational shifts.




Interested candidates kindly mail your resume to:
pooja.rajapurkar2@cognizant.com


Regards,


HR Team

Company Profile

Cognizant (NASDAQ: CTSH) is a leading provider of information technology, consulting, and business process outsourcing services, dedicated to helping the world's leading companies build stronger businesses. Headquartered in Teaneck, New Jersey (U.S.), Cognizant combines a passion for client satisfaction, technology innovation, deep industry and business process expertise, and a global, collaborative workforce that embodies the future of work. With over 100 development and delivery centers worldwide and approximately 221,700 employees as of December 31, 2015, Cognizant is a member of the NASDAQ-100, the S&P 500, the Forbes Global 2000, and the Fortune 500 and is ranked among the top performing and fastest growing companies in the world. Visit us online at www.cognizant.com or follow us on Twitter: Cognizant.

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