Thursday, 14 May 2015
Friday, 8 May 2015
Walk-in for Trainee - Scientific Writing - 9th May 2015 : 9 AM - 25 Opening(s) -Indegene
| Walk-in Details | Date-9th May, Starting Time: 9 AM | ||||||
| Designation | Walk-in for Trainee - Scientific Writing - 9th May 2015 : 9 AM - 25 Opening(s) | ||||||
| Job Description |
Develop content for various deliverables meeting quality requirements
as per client satisfaction metrics, with active guidance from the
manager Responsible to develop content as per the timelines assigned Responsible to follow the best practices in the department regarding - processes, communication (internal & external), project management, documentation and technical requirements like - language, grammar, stylization, content search, summarizing, data conflicts and referencing Participate in assigned training programs and work on assignments as per requirement Participate in client calls as per project requirements Compliance to quality, confidentiality and security: Adhere and follow quality systems, processes and policies Comply to training and specifications | ||||||
| Desired Profile | Pharm D/ M.Pharm Freshers. (2014/2015 pass out only). Understanding of any specialty area of medicine (preferred) or an overall understanding of the medical field. Strong flair and passion for writing. Strong written and verbal communication/presentation skills. Passion for networking. Being up-to-date with the latest technical/scientific developments and relating them to various projects.
|
Medical Writer - Walk-in on 9th May (candidates fm Delhi)
CTC: 2,00,000 - 3,00,000 P.A
Candidate should have excellent standard of writing English
Walk-In on 9th May 15 btwn 9:30 am to 11:30 am at:
Derric Wood:
Unit No. 702,703, 704 Gopal Heights,
Netaji Subhash Place, Pitampura, Delhi,
Near : Netaji Subhash Place Metro Station
Candidate should have excellent standard of writing English
Walk-In on 9th May 15 btwn 9:30 am to 11:30 am at:
Derric Wood:
Unit No. 702,703, 704 Gopal Heights,
Netaji Subhash Place, Pitampura, Delhi,
Near : Netaji Subhash Place Metro Station
- * Research and Write original content for project activities
* Research, develop and write content that is medically & grammatically accurate.
* Attention to detail and high degree of scientific and medical accuracy in medicalwriting
Clinical Research Associate-Embrace Innovations Private limited -Bengaluru/Bangalore
CTC :2,25,000 - 3,75,000 P.A
- Working knowledge in all areas of research including GCP, IRB protocol submission, Notifications and safety reporting.
- Conducting Feasibility assessments at sites for conduct of clinical trial.
- Assisting the investigator for conducting all study related activates, Identification of patients for the study. and follow-up with CRA for various concerns of trial related activities.
- Helping the investigator in achieving the recruitment goals of various trials and planning and conducting the follow-ups of the recruited patients as per study protocol, ICH GCP and all applicable regulatory guidelines
- Assisting the investigators in resolving in DCF's and helping CEVA Documents submission during cardiac related SAE and communicating with medical monitors in respective of any safety issues
- Proven project management abilities with capacity to train on different issues problem solving, mean time updating study related activities and the global news during ongoing trials, able to manage multiple responsibilities without compromising on detail or quality.
- Training the team on the Protocol, Handling and maintaining Study medication, Study related procedures, filling of CRF's.
- Regular update of safety issues in EDC/CRF and notifications to EC and to regulatory body for notifying Appendix11.
- Management and regular update of Trial master file and essential documents.
- Internal Monitoring of the studies conducted at site.
- Data entry, analysis and interpretation.
- Preparing the study report.
- Meet EC Chairperson/Member Secretary and coordinate smooth operations for Submission/Approval/Notification from site.
Coordinate with sites to improve the performance.
APPLY HERE
Thursday, 7 May 2015
Drug Safety Associate Salary
The average salary for a Drug Safety Associate is Rs 279,296 per year.
Most people with this job move on to other positions after 10 years in
this field.
http://www.payscale.com/research/IN/Job=Drug_Safety_Associate/Salary
http://www.payscale.com/research/IN/Job=Drug_Safety_Associate/Salary
Wednesday, 6 May 2015
International Business Development Manager - Clinical Research-TECH OBSERVER-Delhi
-
Establish & maintain positive,profitable relationship with key
personnel in assigned client account to generate business. contributing
to completion of projects in time,generating leads,executing contracts,
RFP/RFI response.
APPLY HERE
Clinical Research Coordinator-TECH OBSERVER -Bengaluru/Bangalore
CTC:1,25,000 - 1,50,000 P.A
-
Recruitment,coordination & follow up of trial subjects, covering
informed consent, adhering to safety and compliance issues;sample
collection & shipment;Administer study drug;Coordination &
management of Clinical Trial;
APPLY HERE
Medical Writing - Trainee ( Fresher )-Quintiles-Bengaluru/Bangalore
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, straightforward bioanalytical study data reports, 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, reports or sections of documents or reports, 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 and/or technical writing/regulatory knowledge, developments and advances in area of drug development/medical and/or technical writing.
Complies with Company SOPs and participates in the implementation of new SOPs.
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/technical writing, such as Good Laboratory Practices (GLP) and other relevant regulatory agencies (e.g. OECD, MHLW).
Careful attention to detail and accuracy.
Must be computer literate.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Dentistry / BHAMS / M-Pharm with post-graduation in clinical research.Bachelors degree in a life science-related discipline, communications, technical writing, or related field; or equivalent combination of education, training and experience. FRESHER
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, straightforward bioanalytical study data reports, 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, reports or sections of documents or reports, 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 and/or technical writing/regulatory knowledge, developments and advances in area of drug development/medical and/or technical writing.
Complies with Company SOPs and participates in the implementation of new SOPs.
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/technical writing, such as Good Laboratory Practices (GLP) and other relevant regulatory agencies (e.g. OECD, MHLW).
Careful attention to detail and accuracy.
Must be computer literate.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Dentistry / BHAMS / M-Pharm with post-graduation in clinical research.Bachelors degree in a life science-related discipline, communications, technical writing, or related field; or equivalent combination of education, training and experience. FRESHER
APPLY HERE
Scientific Writer 2-Novartis Healthcare Pvt. Ltd.-Hyderabad / Secunderabad
- Employment Type - Regular
Job Description - Preparation of the above referenced documents meeting set quality standards and on time for submission to Health Authorities/ Clinical teams / Journals as appropriate. (i.e. complying with standards e.g. CONSORT regarding publication of trial results, complying with journal formatting requirements etc). 2.Publications are acceptable to internal and external authors (no issues with authorship). 3.Publications are acceptable to marketing and other internal customers. 4.Completion of an adequate number of medical and scientific documents (taking into account complexity) per year.
Minimum: Life-science degree or equivalent Good written and oral English skills B.Sc./equivalent with 4 years ClinicalResearch (CR) experience, M.Sc./M.Pharm + 2 years of CR experience, Desired Doctoral degree, Qualification in Medical Sciences (MBBS/MD/equivalent) PhD + 1 year of CR experience, MBBS/equivalent + 1 year of CR experience.
APPLY HERE
Central CRA- Novartis Healthcare Pvt. Ltd.-Hyderabad / Secunderabad
- Responsible for central remote monitoring of assigned clinical trial(s) executed by GBS Clinical
Trial Services on behalf of Novartis Organizations. Use online data
sources to review patient data for consistency, plausibility and
completeness. Early identification of potential risks, safety and/or
quality issues and trigger required follow-up actions. Ensure high
quality and complete data is available.
APPLY HERE
Tuesday, 28 April 2015
Manager, IQS Scientific Operations-Novartis Healthcare Pvt. Ltd. -Hyderabad / Secunderabad
-
Support operational and functional excellence across IQS functions by
focusing on one or more of the following areas: Common processes,
practices, and systems to ensure efficiency, quality, compliance and
financial support (including definition, implementation and tracking of
metrics/KPIs) Review and consolidation of project resource requirements
across IQS functions, define internal and external sourcing strategies
solutions to best utilize IQS functional capabilities and meet the
clinical programs goals in line with departmental budget. Hiring, on
boarding, and training programs for IQS functions to attract and develop
talents. Knowledge management, communication, and innovation
MSc or equivalent experience in mathematics, statistics, computer science, or health sciences/related field Fluent English required (oral & written) At least 6 years relevant experience (or equivalent breadth of Pharmaceutical experience) including several years in a project functional lead role Good understanding of clinical development, quality and regulatory standards and policies relevant to Data Management, Statistical Reporting, Biostatistics, MedicalWriting (e.g. GCP, ICH) Experience with and good knowledge of the design of randomized controlled clinical trials. Successful experience working in cross-functional teams and management of projects Ability to effectively lead major non-clinical initiatives requiring clinical trial planning, execution, analysis and reporting expertise. High degree of results-orientation and ability to execute Must be able to organize, prioritize and work effectively in a constantly changing environment and motivate the team to do the same Experience in leading operations and innovation Strong communication and collaboration skills.
APPLY HERE
Senior Medical Writer-Novartis Healthcare Pvt. Ltd. -Hyderabad / Secunderabad
- To write,
edit and/or manage the production of high quality clinical
documentation for submission to regulatory authorities in support of
marketing applications.
Minimum university life science degree or equivalent Languages: Excellent written and spoken English. Experience/Professional requirement: 1. At least 2 years medicalwriting experience. 2. Good knowledge of statistics and data interpretation and presentation skills. 3. Good knowledge of clinical documentation. 4. Good knowledge of regulatory requirements. 5. Good knowledge of drug development.
APPLY HERE
Associate Medical Writer-Quintiles -Bengaluru/Bangalore
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, straightforward bioanalytical study data reports, 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, reports or sections of documents or reports, 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 and/or technical writing/regulatory knowledge, developments and advances in area of drug development/medical and/or technical writing.
Complies with Company SOPs and participates in the implementation of new SOPs.
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/technical writing, such as Good Laboratory Practices (GLP) and other relevant regulatory agencies (e.g. OECD, MHLW).
Careful attention to detail and accuracy.
Must be computer literate.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Dentistry / BHAMS / M-Pharm with post-graduation in clinical research.Bachelors degree in a life science-related discipline, communications, technical writing, or related field; or equivalent combination of education, training and experience. 1 - 2 years experience in Medical Writing.
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, straightforward bioanalytical study data reports, 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, reports or sections of documents or reports, 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 and/or technical writing/regulatory knowledge, developments and advances in area of drug development/medical and/or technical writing.
Complies with Company SOPs and participates in the implementation of new SOPs.
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/technical writing, such as Good Laboratory Practices (GLP) and other relevant regulatory agencies (e.g. OECD, MHLW).
Careful attention to detail and accuracy.
Must be computer literate.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Dentistry / BHAMS / M-Pharm with post-graduation in clinical research.Bachelors degree in a life science-related discipline, communications, technical writing, or related field; or equivalent combination of education, training and experience. 1 - 2 years experience in Medical Writing.
APPLY HERE
Opening for Research Associate Toxicology with Evalueserve-Evalueserve.com Pvt. Ltd -Gurgaon
Job Description
To extract, analyse and report data from various toxicology-related databases like TOXNET, HSDB, PubMed, Medline, ScienceDirect etc.
To evaluate quality of different toxicity studies
To identify the critical toxicology data for writing a hazard summary or assessment of a chemical.
To prepare research reports / dossiers according to the international regulatory guidelines
Mandatory Skill Set required
Thorough understanding of various types of basic toxicological principles and toxicological studies
Knowledge of OECD/FDA/EPA guidelines for preclinical toxicity studies
Knowledge of various toxicology/pharmacology databases like TOXNET, ECOTOX, PubMed, e-Chemportal etc.
Knowledge of preclinical safety screening studies as practiced in industry
Good interpersonal skills and communication (both written and verbal) skills
Ability to ensure that tasks within areas of responsibility are completed accurately in a timely manner
Ability to practice attentive and active listening skills
Ability to identify pro-active ways to contribute to firms goals & mission
Challenging current thinking by implementing new ways of working
To extract, analyse and report data from various toxicology-related databases like TOXNET, HSDB, PubMed, Medline, ScienceDirect etc.
To evaluate quality of different toxicity studies
To identify the critical toxicology data for writing a hazard summary or assessment of a chemical.
To prepare research reports / dossiers according to the international regulatory guidelines
Mandatory Skill Set required
Thorough understanding of various types of basic toxicological principles and toxicological studies
Knowledge of OECD/FDA/EPA guidelines for preclinical toxicity studies
Knowledge of various toxicology/pharmacology databases like TOXNET, ECOTOX, PubMed, e-Chemportal etc.
Knowledge of preclinical safety screening studies as practiced in industry
Good interpersonal skills and communication (both written and verbal) skills
Ability to ensure that tasks within areas of responsibility are completed accurately in a timely manner
Ability to practice attentive and active listening skills
Ability to identify pro-active ways to contribute to firms goals & mission
Challenging current thinking by implementing new ways of working
APPLY HERE
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