Manager Client Services,1-2 years of Clinical Research Experience with MBA/ PGDM may apply @ Indegene Lifesystems Pvt. Ltd. - Bangalore D 10

Job description

Position Details : Manager Client Services

Designation : Manager Client Services

Experience : 0 to 2 years

Position Type : Full Time

Functional Area : Program management

Education : M.B.A/PGDM

Work Location : Bangalore

Job Description 
1. Should be responsible for delivery of projects on time and as per the quality expectations of the client

2. Strive to reduce turnaround time on an ongoing basis

3. Liaise and facilitate transfer of information between clients, business development teams, and delivery teams, in accordance with the established guidelines/processes/documentations

4. Assist the sales team in acquiring key orders or accounts by way of proposal development, on-/off-site presentations, etc.

5. Train and develop teams for projects as required 

Desired Profile 

1. Minimum 3 to 6 years of experience in pharmaceutical companies

2. Experience in any of the following functions: medical services/medico-marketing/health care/project management (preferred)

3. Strong people management skills

4. Strong written and verbal communication/presentation skills

5. Passion for networking

6. Keeping updated with the latest technical/scientific developments and relating them to various projects



Soft Skills 

· Client focus

· Result orientation

· Communicating with Impact

· Team player

· Process oriented

Apply online

Fresher M Pharm/ BDS/ MBBS apply for Clinical Trials Analyst @ Indigene, Banglore, "D3"

Job description

Designation : Clinical Trial Analyst 

Experience : 0 to 2 years 

Position Type : Full Time 

Functional Area : Scientific Content 

Education  : B.D.S, M.Pharm, MBBS 

Work Location : Bangalore 

Job Description 

1.To Review of various clinical trial protocols and source documents.

2.Clinical trial data analysis, tagging and updating the database.

3.Advise data management staff on trial parameters, database designs, and validation of
critical data. 

4.Reports progress and changes in clinical trials.

5.Statistical analysis and competitive analysis of trial results.

Desired Profile 

1.Should have a qualified MBBS, BDS, M Pharm Degree.

2.A strong educational background in clinical research. 

3.Computer skills including use of Microsoft word, excel and power point.

4.In depth therapeutic and clinical research expertise as well as knowledge of
GCP/ICH and applicable regulatory guidelines. 

Soft Skills

·Client focus 

·Result orientation

·Communicating with Impact

·Team player

·Process oriented

About the Company: 

Indegene is a leading provider of R&D, commercial and marketing solutions to global pharmaceutical and healthcare organizations. We partner with clients to drive both productivity and revenues by delivering better patient outcomes, optimizing cost, enhancing R&D agility, and improving sales and marketing effectiveness. We apply deep scientific knowledge, flexible delivery models, proprietary technology, and a client-centric approach to drive transformational initiatives.

With offices in US, UK, China, India, and Australia, Indegene can partner globally with clients; leverage a global talent pool of clinicians, technologists, creative specialists, domain experts, and business process specialists; deploy global infrastructure assets; and harness global healthcare knowledge to solve client challenges. For more information, visit www.indegene.com

Apply to Company Website

Any Graduates required for Mechanical Maintenance ( formulation Plant ) Pharma Company, D2

·        Specialization :Design Engineering , Engineering , Industrial Engineering , Plant Maintenance

·     Job Function :Production / Manufacturing / Maintenance / Packaging

·      Industry :Consumer Durables / FMCG , Manufacturing / Industrial

·      Vacancies :25

• Location : Ahemedabad , Bengaluru / Bangalore , Delhi , Delhi / NCR , Gurgaon
• 
  
• Experience: 0 to 3 yrs
• CTC: Rs. 15,10,000 - 30,10,000 p.a.

    Experience required: 0-3 years

    Education Requirement: Graduates in any discipline

   Company Profile:  Impact India Private Limited

     Industrial Manufacturing Company

Job vacancy for the post of CLINICAL RESEARCH COORDINATOR @ BANGALORE/MYSORE LOCATIONS - Eligibility - Any Clinical Professional with minimum 6 month experience preferably in a Endocrinology Trial - Interested candidates may walk in @ below mentioned address or mail your CV to cliniindiabangalorejob@gmail.com writing "Your experience in subject line" - D9

ADDRESS - 
CLINI INDIA BANGALORE
II FLOOR, PRESTIGE OMEGA BUILDING,
NEAR VYDEHI INSTITUTE OF MEDICAL SCIENCE,
OPP. TESCO OFFICE,
WHITEFIELD MAIN ROAD,
BANGALORE
Contact no. 080 959 739 22

WALK IN DATE : 19, 20 & 21 JUNE.14 BETWEEN 10:00 a.m. to 4:00 p.m.

Medical Writer- I Vacancy in PARAXEL "D3"

Role: Medical Writer- I @ Banglore

Job Summary : As a Medical Writer Iyou would work on Clinical Study Documents, mainly Narrative

Writing.

Key responsibilities

Under divisional supervision as needed, the Associate Medical Writer will research, create, edit, and coordinate the production of clinical documents associated with regulatory submissions.

 The Medical Writer 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 may serve as primary technical contact with the client under appropriate divisional supervision.

The position is focused but may not be limited to the handling of documents and communication associated with the submission to Independent Ethic Committee(s) and the local Regulatory Authorities in India or other global regulatory bodies.

 Maintain a positive, results orientated work environment, building partnerships and modeling teamwork, communicating to the team in an open, balanced and objective manner.

Write clinical documents associated with submissions to regulatory authorities including but not limited to Study protocols, Informed consent documents, Clinical study reports, Submission forms for regulatory bodies.

 Prepare clinical study reports to regulatory standard for e-submission. • Assist with preparation and compilation of appendices to clinical study reports.

May supervise collection of materials by Medical Writing Assistant for assembly of client deliverables and for filing appropriately in Central Files, project files and Medical Writing archives.

Ensure document content and style adheres to appropriate regulatory guidelines, and complies with company or client SOPs and style guidelines, Teamwork within Medical Writing and the Unit

 Attend internal technical team meetings

May participate in divisional or interdivisional process improvement and training initiatives.

Serve as the Medical Writing representative on assigned project teams.

 Job Qualifications The ideal candidate for this role would be a PhD, MBBS (or equivalent Indian Medicine degree), BDS/MDS, MSc with excellent English Language/Communication skills (the latter is mandatory).

Experience: 1 to 3 years corporate regulatory medical writing is ideal for this role. Prior/Academic experience of literature, own research, magazine or newspaper writing would be an advantage. 

To Apply Directly

Fore Medical Writing Training Courses

Apply for Clinical REsearch Associate - CRA 1 / CRA 2 / Sr CRA in Quintiles ( Bangalore / Mumbai / Delhi ) "D6"

Job description

The CRA conducts monitoring visits for assigned protocols and study sites. Overall responsibilities are to ensure that the study is being conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.

- Performs site selection, initiation, monitoring and close out visits in accordance with contracted scope of work and good clinical practices.
- Provides monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
- Completes appropriate therapeutic, protocol and clinical research training to perform job duties.
- Administers protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluates the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalates quality issues to Clinical Team Lead and/or Line Manager
- Manages the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, CRF completion and submission, and data query generation and resolution.
- Creates and maintains appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation.
- May provide training and assistance to more junior clinical staff.

Qualifications :
- Degree (Bachelor's or Master's) in a scientific discipline
- The candidate must be willing to travel for at least 10 to 12 days in a month, though not necessarily continuous.
- Computer skills including use of a laptop computer, knowledge of Microsoft Word, Excel and PowerPoint preferred.
- Basic knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
- Strong written and verbal communication skills including good command of English required.
- Excellent organizational and problem solving skills.
- Effective time management skills and ability to manage competing priorities.
- Ability to establish and maintain effective working relationships with co-workers, managers and clients
- Training as Clinical Research Associate in Quintiles as per Quintiles India Clinical Operations Training policy or equivalent work experience in the CRO/pharmaceutical industry

To start career in Clinical Research as a Fresher , Apply for- Clinical Trial Analyst Position- "D5"

Job Title: Clinical Trial Analyst

Experience : 0 to 2 years

Position Type : Full Time

Functional Area: Scientific Content

Education : B.D.S, M.Pharm, MBBS

Work Location : Bangalore

Job Description

1.To Review of various clinical trial protocols and source documents.

2.Clinical trial data analysis, tagging and updating the database.

3.Advise data management staff on trial parameters, database designs, and validation of
critical data.

4.Reports progress and changes in clinical trials.

5.Statistical analysis and competitive analysis of trial results.

Desired Profile

1.Should have a qualified MBBS, BDS, M Pharm Degree.

2.A strong educational background in clinical research.

3.Computer skills including use of Microsoft word, excel and power point.

4.In depth therapeutic and clinical research expertise as well as knowledge of
GCP/ICH and applicable regulatory guidelines.

Soft Skills

·Client focus

·Result orientation

·Communicating with Impact

·Team player

·Process oriented

Apply Now

Openings for Pharmacovigilance Post for Banglore locations.For professional with 9 months-3+ Years of Exp in Pharmacovigilance "D7"

Openings for Pharmacovigilance Post for Banglore locations.
Eligibility : 9 months-3+ Years of Exp in Pharmacovigilance
Education: Bachelors or Master Degree or BDS or MBBS

Please forward the CV's to healthcare_research@yahoo.in

Clin Project Mgr

Clin Project Mgr
Quintiles Transnational - Bangalore, Karnataka

PURPOSE Manage the execution of the assigned regionally-based clinical study(ies) per Contract, from initiation through to closeout. Ensure that all clinical study management and project deliverables are completed to the Sponsor’s satisfaction, ensuring quality deliverables on time and within budget and in accordance with SOPs, policies and practices. RESPONSIBILITIES  Manage and co-ordinate efforts of cross-functional project teams to support milestone achievement and to manage study issues and obstacles and ensure consistent use of study tools and training materials and compliance with standard processes, policies and procedures.   Develop study management plans, together with team assignments and accountability and oversight of database maintenance.   Serve as primary project contact with Sponsor to ensure communication is maintained and reporting schedules are adhered to.   Collect information on team performance against contract, customer expectations, and project baselines.   Lead problem solving and resolution efforts to include management of risk, contingencies and issues.  Identify quality issues within the study to implement appropriate corrective action plans. Escalate findings and action plans to appropriate parties.   Provide input for the development of proposals for new work and manage project budgets.   Provide input to line managers of their project team members’ performance relative to project tasks.   Prepare and present project information at internal and external meetings.   Participate in proposal development and in the bid-defense process with guidance and supervision.   Ensure high performance and efficiency of the clinical team through the scheduling of co-monitoring/accompanied site/visits and ongoing mentoring of CRA team. For more info visit at mentioned link

Associate Business Development Director

Associate Business Development Director
Quintiles Transnational - Bangalore, Karnataka

PURPOSE Secure and retain business through professional, consultative, proactive sales activities directed at decision-makers and decision influences at existing and new clinical sponsors. RESPONSIBILITIES • Actively prospect and leverage potential new business opportunities within specified customer account(s). • Cultivate strong, long-term relationships with key decision-makers within Account and develop in-depth knowledge of the customer organization. • Maintain general knowledge of all Quintiles services for appropriate cross-sell opportunities. • Aggressively pursue awareness of competitive activities, positioning and pricing, which includes specific reasons for awards and non-awards. • Identify and respond to customer needs in order to define potential opportunities. Propose appropriate strategy/solution to customer. For more info visit at mentioned link

Job for Sr. Clinical Data Coordinator/Assistant Manager, CDM/Associate Manager

Job for Sr. Clinical Data Coordinator/Assistant Manager, CDM/Associate Manager in Quintiles

Job Description
• The Sr. Clinical Data Coordinator provides comprehensive data management expertise to Data Management.
• The position also requires to provide efficient, quality data management products that meet customer needs.  Provide leadership either in the role of the Data Operations Coordinator (DOC), or in a leadership role in a specific Department task.
• Serve as Data Operations Coordinator (DOC) for one or two global studies with fewer than 10 operations staff (excludes DE), or serve in a leadership role to a specific DM Task.   (See Responsibilities Document for role description)
• Manage delivery of projects through full data management study life-cycle (with minimal guidance)

For more info visit at mentioned link

QA Analyst

QA Analyst
Xerox - Bangalore

Title: QA Analyst Location: Bangalore May perform one or more of the following: Develops and implements total quality management (TQM) programs and initiatives. Conducts audits and reviews/analyzes data and documentation. Develops, implements, and leads key process improvement efforts and influences cross-functional efforts. Assists in the development of systematic approaches for assuring high quality services. Identifies the interface of key activities within and between the functions of the organization. Focuses on the factors such as resources, methods, and materials that will improve key activities of the organization. Integrates and aligns the processes that will best achieve the desired results. Makes continual improvement of products, processes and systems. For more info visit at mentioned link

Research Operations Assistant

Research Operations Assistant 
PAREXEL International - Bangalore

Job Description : The role of the Research Operations Assistant (ROA) is to support all site management team members on local billable administrative tasks. The ROA has a basic understanding of Clinical Operations service offerings and processes. Key Accountabilities Track, scan, code and send documents to the relevant study Work In Progress (WIP) area of PMED or send wet-ink documents to the respective Central Files office location as per the Central File Maintenance Plan (CFMP) Complete the set-up, configuration and distribution of Investigator Site Files (ISF) under the supervision of the local site management team members Support local site management team in the preparation of site-specific documents and cover letters Copy documents or coordinate copying if done by a vendor Distribute study documents to sites and/or local authorities (e.g. via courier shipments) as required Assist with quality checks of submission packages (as applicable) Assist with the organization of translations of study document (e.g. contacting translation company, requesting approval via Oracle, following up with translation company to ensure timely delivery) Check incoming faxes and escalate any urgent faxes (e.g. reported Serious Adverse Events) to CMA Assist CMA with payment/invoice processing including internal follow up with payment specialists in Finance Assist local site management team members with tracking/maintenance of the Clinical Trial Management System (CTMS) and study specific site trackers (if applicable) Assist with the collection of internal signatures for site documents (e.g. confidentiality agreement or clinical site agreements) within PAREXEL Assist with logistics for in-house and on-site audits. For more info visit at mentioned link

Medical Writer II

Medical Writer II 
PAREXEL International - Bangalore

Job Description : Essential Function 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. Qualifications : Attend internal technical team and client team meetings as required. May provide guidance to less experienced departmental members. 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. May participate in departmental or interdepartmental process improvement and training initiatives. May participate in development of formats, templates and general guidelines for clinical documentation and workflow procedures. Assist in the development of departmental SOPs. Keep abreast of professional information and technology through workshops and conferences, and ensure the appropriate transfer of that information to the department. For more info visit at mentioned link

Walk in for Fresh B.Pharm, B.Sc, M.Pharm, M.Sc (60 posts) at XL Health

Walk in for Fresh B.Pharm, B.Sc, M.Pharm, M.Sc (60 posts) at XL Health - A United Health Group Company

Job Description: 
Educational Qualification - BDS, BSC/M. Sc.(Bio-tech, Microbiology, Zoology), B. Pharm., M. Pharm., B.E in Bio Technology, BHMS, Ayurvedic, Homeopathy, Physical Therapist, Occupational Therapist, Nurses, trainee Medical Transcriptional/ OJTs, and other candidates with knowledge of human anatomy & physiology.

Interview  will be held on Monday ie on 28-april-2014 at 9.00 a.m. on Friday

Venue of Interview:
XLHealth Corporation India Private Limited
(formerly known as XLCare Information Systems Pvt. Ltd.)
XLHealth Corporation India Pvt. Ltd.,
#4, SALARPURIA SAPPHIRE,
Hosur Main Road, Adugodi,
Bangalore - 560034

For more info visit at mentioned link

Senior Laboratory Technicians/ Laboratory Technicians

Senior Laboratory Technicians/ Laboratory Technicians/ Accountant 
National Tuberculosis Institute - Bangalor


 Senior Laboratory Technicians 

MSc (Microbiology) or MSc (Medical Laboratory Technology) with DMLT. Experience : A Minimum of 3 years’ experience of working in a laboratory with specific knowledge of setting up culture and sensitivity of Mycobacterium tuberculosis in both solid (LJ) and especially Liquid culture systems (MGIT). Previous experience of working in RNTCP is an added advantage Knowledge on molecular techniques, genetic sequencer will be an added advantage Knowledge of Computer 
 
Rs. 25,000 

 Laboratory Technicians 

BSc (Microbiology) or BSc (Medical Laboratory Technology) with DMLT. Experience : A Minimum of 3 years’ experience of working in a laboratory with specific knowledge of setting up culture and sensitivity of Mycobacterium tuberculosis in solid (LJ), smear microscopy and media preparation. Previous experience of working in RNTCP is an added advantage.

Rs. 18,000

For more info visit at mention link

Director, Data Management - Bangalore

Director, Data Management - Bangalore

Description

Due to continued growth, PPD is hiring a Director of Data Management to be based in Bangalore to support our global projects. This is an exciting opportunity to join a multinational American based CRO that is growing and expanding in India. Joining our global Data Management team, we employ the technology, processes and expertise that best meet the needs of our client’s project with PPD’s Clinical Data Management solutions. Across a broad range of therapeutic areas and quantitative methods, PPD has extensive data management experience for Phase I-IV clinical trials.

 

This is a great opportunity for a strategic and operationally focused Director to join at an exciting time, and overseeing clinical data management projects on a global scale.

 

Duties and Responsibilities of the Director, Data Management will include:

• Actively engaging in business development activities to strategically drive the growth of this function on a global scale with existing and new clients.
• Providing high-quality technical support on project.
• Providing leadership and coaching to the department.
• Providing substantive advice on strategy, regulations and industry best practices; demonstrates subject matter and therapeutic area expertise.
• Demonstrating strong collaboration with internal stakeholders, internal and external clients; effectively manage projects to deliver quality products in agreed timelines; demonstrate flexibility and adaptability, as applicable, to client deliverable and needs.
• Ability to work on extremely complex problems where analysis requires evaluating various factors
• Providing high level oversight and direction to the Data Management group to include departmental budgets, personnel and resource management to ensure key operational business targets are met including financial and utilization.

For more info visit at mentioned link

Medical Writing - Intern-1407773 @ Quintiles, For freshers @ Bangalore "D"

 

Job Description - Medical Writing - Intern (1407773) Job Description  Medical Writing - Intern-1407773 Description   PURPOSE Assists senior medical writing staff in the preparation of study reports, submissions, or other documents for either internal Quintiles customers or external clients, for investigational drugs, biologicals, or medical devices. Participates in project teams and may lead specific straightforward or small tasks, consulting senior staff as necessary.   RESPONSIBILITIES • Supports Medical Writing senior staff in managing client requests. Examples include but are not limited to the following: writing patient narratives, checking document edits, checking documents for consistency, adapting generic document shells to project specifications, assisting with document compilation, and entering numbers into in-text tables. May also draft text for simple documents or sections of documents, with guidance of senior staff. • Identifies project needs, tracks project timelines and implements client requests, with senior review. • Interacts with internal clients. May have some external interactions, mostly directed by senior staff. • Takes responsibility for managing day-to-day workload for assigned tasks, in collaboration with senior staff. • Keeps abreast of current data, trends, medical writing/regulatory knowledge, developments and advances in area of drug development/medical writing. • Complies with Company SOPs and participates in the implementation of new SOPs. All responsibilities are essential job functions unless noted as nonessential (N).   REQUIRED KNOWLEDGE, SKILLS AND ABILITIES • Excellent standard of written English, and ability to communicate fluently and effectively in English, both in writing and verbally. • Ability to work on several projects at once while balancing multiple and overlapping timelines. • Ability to assess workload and suggest prioritization to senior staff. • Demonstrated abilities in collaboration with others and independent thought. • Knowledge of regulations relevant to medical writing. • Careful attention to detail and accuracy. • Must be computer literate. • Ability to establish and maintain effective working relationships with coworkers, managers and clients Qualifications   MINIMUM REQUIRED EDUCATION AND EXPERIENCE • Bachelor's degree in a life science-related discipline or equivalent combination of education, training and experience Primary Location : IND-Karnataka-Bangalore Organization : IND02 - India - CDS/Product Devel

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