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Pharmacist job notification for lucknow UP

 

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Pharm D job vacancy - Clinical trial coordinator

 Applications are invited from eligible candidates for appointment to various posts under the following short term research projects at Malabar Cancer Centre, Thalassery.

Project No-1: To establish a ready network of clinical trial units across the National Cancer Grid to promote multi-centric collaborative research in the field of drug and device development Biotechnology Industrial Research Assistance Council(BIRAC), Govt of India. 

Project No -2: Design and development of ultrasonic transducer probes for medical imaging Ministry of Electronics & Information Technology (MeitY), Govt of India.

Interested candidates possessing the required qualification may fill the online application, in the prescribed format by 10th September 2022 till 5 pm. Selection will be based on the performance in written test and/or interview. In case the number of candidates is large, only shortlisted candidates will be called for interview. 

SN Post Essential Qualifications Experience Maximum age limit Remuneration/ Month No. of vacancy 1. Clinical Trial Coordinator (Project No-1): 

Pharm D/ MPharm/BDS/MPH/MSc(Biostati stics)/ MSc Clinical Research /Post Graduate Diploma in Clinical Research/ MSc Nursing. 

1 year experience in clinical trials or in a Research project or in a funded research project or Pharma sponsored or in Industry supported trails 30 years Rs.30,000/- 01 

2. Clinical Research Assistant (Project No-2): 

MSc Nursing Nil 30 years Rs.32,000/- 02 

3. Data Entry Operator (Project No-2):

 Degree with certificate Course training in computer application One year experience in data entry work 30 years Rs.16,000/- 01

Terms & Conditions: 

1. The post is to be filled up only on purely temporary basis based on the project duration. The duration of an appointment will be one year. The extension will be based on the performance of the candidates.

2. Above said post will be stationed at Malabar Cancer Centre, Thalassery.

3. Since the post is purely temporary, the incumbents selected will have no claim for regular posts and benefits.

4. Applications will be screened and selected candidates will be called for interview. Application received after the due date will not be considered under any circumstances. Details regarding the interview date will be informed later. There may be a screening tests if the number of candidates more than 5 per post. The marks obtained in screening test will not be used for selection except in case of tie in interview. 

5. Any attempt at influencing any official of MCC will be a straightforward reason for outright rejection of the application. Such candidates will be debarred for a period of 5 years from applying to any post in MCC.

6. No TA/DA etc. will be given to attend the Interview or joining of post and out Stationed candidate should make his/her own arrangement for stay for interview and joining of post, if offered.

7. Qualification and experience should be from a recognized University or organization (Recognized by Central or state Government).

8. Age will be calculated as on 1st January of the year. ie 01-01-2022.

9. The decision of Director is final in all aspects of recruitment.

10.Canvassing in any form will lead to automatic disqualification. Candidates are advised to desist from such unholy practices.

How to apply: 

1. Candidates should apply ONLINE through our website www.mcc.kerala.gov.in.

2. Please assure that you have the following before proceeding to Online Registration.  Your photograph in digital form with the following specifications; Maximum Image Size: 30Kb Image Dimension: 150W X 200H px Image Type: .jpg format  Reference number for application fee is Rs. 50 / - for SC / ST category and Rs. 250 / - for others. The application fee shall pay online through the payment gateway system provided in the online Application.

3. The last date of submission of ONLINE application 10th September 2022 till 5 pm.

4. Candidates claiming fee concession/exemption, a copy of SC/ST Certificate from the competent authority, shall be submitted at the time of interview. Else the candidate may pay the pay for the general category.

5. The applications that are not complete in all respect will not be considered and no individual intimation will be given.

6. Selection will be based on qualification and experience and performance in the Test/Interview. Claims in respect of Qualifications, Experience, etc. should be supported by copies of relevant documents; Candidates should produce the originals at the time of interview.

7. The application will be screened and eligible candidates will be informed through email (with date & venue) to attend the interview. Candidate should provide proper contact email ID for communication. Candidates are advised to visit our website www.mcc.kerala.gov.in regularly for updates/ notices and announcements..

8. Qualification, experience prescribed by MCC, should be strictly followed and applications without any of them will be rejected.

9. The Director-MCC will hold the right to reject any application without any information 

Post of Junior Research Fellow

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JOB VACANCY AS SCIENTIST FOR PHARM D

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VACANCY FOR THE POST OF ASSOCIATE RESEARCH ANALYST AT CLARIVATE ANALYTICS, CHENNAI, INDIA

Job ID: JREQ100726

Job Title: Associate Research Analyst

Job Location: Chennai, India

Job type: Full time

About Clarivate Analytics:

Clarivate Analytics clients are the trailblazers and risk takers who come up with life-changing ideas. We’re looking for our own trailblazers to help us keep providing clients some of the world’s most trusted brands, spanning scientific and academic research, patent analytics, pharmaceutical and biotech intelligence and IP management.

We’re an independent owned company with a rich heritage and a bold entrepreneurial mission. If you’re excited by the thought of helping people and organizations go from new ideas to life-changing innovations faster, we’re excited to consider you for a position at Clarivate.

The Drug Information department is part of the Clarivate Analytics’ Ip & Science Editorial Operations Group and comprises several teams responsible for the daily collection, synthesis and maintenance of data relating to investigational and marketed drugs, as well as the companies developing them. These records form a core element of the Cortellis and Thomson Pharma Partnering drug information platforms.

Drug Info News & Pipeline team comprises two internal processes: News – the team scans and processes all relevant press releases from the industry, updates the products with the drug and company information identified. Information is updated within 24 to 48 h of the release. Pipeline Clean-up – the team actively seek out information about a company’s current pipeline (company’s drug development portfolio), analyze, cross reference and update all new or previously unknown information in the drug records from various sources, which includes company websites, presentations, Bio conferences, publications, journals, government websites, clinical trial repositories, and other possible internet sources. 

Essential Responsibilities:

v Accountable for the delivery of weekly database filling milestones.

v Ensure quality standards are observed.

v Ability to understand and interpret complex and detailed Forecast related information from source material

v Ability to research and synthesis scientific information

v An inquisitive, analytical mind with strong problem-identification and -solving skills

Educational Qualification: M.Pharm / B.Pharm / Pharm D

Experience: 0 - 2 years (Freshers are also eligible)

Last date to apply: 18th January, 2018

VACANCY FOR THE POST OF SCIENTIFIC SPECIALIST AT PAREXEL, BENGALURU

Job ID: 39589BR

Job Title: Scientific Specialist

Job Location: Bengaluru

Key Accountabilities:

Specialized Knowledge:

v Demonstrate sufficient understanding of department’s service offerings in order to:

ü Ensure that discussions with client are informed, appropriate, and consistent with MedCom’s service offerings

ü Contribute to client solutions

v Be familiar with and comply with all departmental procedures related to project delivery and tracking, promote adoption of these procedures by others, and recommend appropriate enhancements for efficiency

v Develop and maintain in-depth knowledge of client products and therapy areas on assigned accounts

v Develop and maintain in-depth knowledge of relevant industry guidelines (eg, Good Publications Practice), apply these to assigned projects and promote adherence by others

v Identify technical or process issues that are relevant to project delivery, and initiate, or work with other team members to initiate, appropriate actions

v Creatively and proactively apply specialist knowledge when working as part of a proposal and pitch development team

Project Execution and Success:

v Undertake writing and editing to develop high-quality scientific content

v Prioritize own work and manage project schedule to meet delivery deadlines

v Be familiar with and work within project scope (specification and budget hours) and objectives. Monitor project progress, scope changes, and own hours sufficient to flag changes in scope to project lead, and proceed accordingly

v Interpret scientific data accurately and appropriately

v Maintain familiarity with client objectives and messages and produce output consistent with these

v Undertake necessary research on topics relevant to assigned projects and maintain familiarity with available information sources

v Liaise with all opinion leaders/authors or other external parties in such a way as to foster strong and positive relationships and to ensure project success

v Identify issues that may affect project delivery and take independent action or liaise effectively with Manager and other team members, as appropriate, to resolve project issues

v Follow up on all assigned actions and proactively communicate status

v Maintain familiarity with and adhere to departmental SOPs (those related to quality control and all others)

v Seek opportunities to maximize project efficiency and make recommendations or take actions as appropriate

v Provide guidance to other team members on technical or process issues as necessary

v Provide mentorship and coaching of other team members, as directed

v Communicate effectively and sensitively with team members across all functions

v Participate in team discussions and meetings and contribute actively

v Proactively use knowledge and experience to for the benefit of project delivery and business success

Client Management:

v Proactively assess project needs and work to identify how these can be best met, to the benefit of client satisfaction and project profitability

v Identify complex technical and process issues and work with internal cross-functional teams, client, and/or external bodies to resolve them

v Be alert to opportunities to develop follow-on business

v Actively communicate and manage changes in project scope

v Maintain high level of client satisfaction with all interactions and deliverables

v Undertake discussions with client so as to actively manage timelines and expectations, maintaining client satisfaction throughout

Skills:

v Intermediate computer and Internet skills, including knowledge of MS applications such as Excel, Word, and PowerPoint

v Strong oral and written communication skills

v Strong problem-solving skills

v Technical expertise:

ü Ability to acquire and apply specialized therapy area knowledge

ü Ability to interpret and organize scientific data

ü Ability to understand and implement marketing messages

Qualifications

Education

Degree and a higher degree in Life Sciences, Pharmacy, or Medicine (BSc, BA, Pharm D, PhD, MD)

Language Skills

Proficient use of English language

Work Experience

Prior experience in a similar role, preferably within a medical communications agency environment.

Last date to apply: 18th January, 2018

MULTIPLE VACANCIES UNDER DEPARTMENT OF HEALTH, MEDICAL AND FAMILY WELFARE, TELANGANA

VACANCY FOR THE POST OF CLINICAL RESEARCH ASSOCIATE (CRA) AT PRA HEALTH SCIENCES, MUMBAI

Job ID: 2017-43930

Job Title: Clinical Research Associate (CRA)

Job Location: Mumbai, India

Job Overview:

The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

Responsibilities

ü  Applies knowledge of PRA’s policies and procedures

ü  Demonstrates excellent written and oral communication

ü  Demonstrates excellent knowledge of ICH/GCP

ü  Displays ability to manage investigative sites to facilitate trial deliverables

ü  Demonstrates ability to escalate issues appropriately 

ü Conducts monitoring to confirm subject safety and data integrity

ü Describes and demonstrates the principals of IP accountability

ü Identifies scientific misconduct at the site level

ü Demonstrates working knowledge of Microsoft Office applications, Clinical Trial Management Systems, IVRS/IWRS and Electronic Data Capture platforms

ü  Mentors CRAs new to the position or company

ü  Serves as an observation visit leader

ü  Conducts monitoring evaluation visits

ü Assists team lead in the development of trial tools or documents

Qualifications

ü  Read, write and speak fluent English; fluent in host country language required.

ü  2+ years of clinical monitoring experience required

ü  Knowledge of ICH and local regulatory authority regulations regarding drug

ü Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required

ü  Clinical research experience

ü  Knowledge of ICH and local regulatory authority regulations regarding drug

ü  An advanced degree (e.g., M.S., M.B.A., Pharm D, etc)

ü Experience in monitoring all trial components (PSSV to COV)

ü  Experience in coaching/mentoring other CRAs

Last date to apply: 15^th December, 2017

VACANCY FOR THE POST OF SENIOR DRUG SAFETY ASSOCIATE AT COVANCE, MUMBAI

Job ID: 2017-14725

Job Category: Clinical operations

Position type: Full time

Job Overview

ü Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to:

ü Entry of safety data onto adverse event database(s) and tracking systems

ü Review of adverse events for completeness, accuracy and appropriateness for expedited reporting

ü Write patient narratives

ü Code adverse events accurately using MedDRA

ü Determine expectedness/listedness against appropriate label

ü Identifies clinically significant information missing from initial reports and ensures its collection

ü Ensure case receives appropriate medical review

ü Prepare follow-up correspondence consulting the medical staff accordingly.

ü Ensure all cases that require expediting reporting to worldwide regulatory agencies are processed swiftly and appropriately within required timelines

ü Reporting of endpoints to clients, regulatory authorities, ethics committees, investigators and Covance project personnel, if required, within study specified timelines

ü Provide independent QC of AE reports for other members of the group

ü May execute routine quality review of AE reports and aggregate reports for other members of the group ensuring that case processing and data quality meet global regulatory compliance needs including audit support.

ü Maintain a strong understanding of Covance’s safety database conventions or client-specific database conventions, as appropriate.

ü Participate in signal detection, trend and pattern recognition activities, as appropriate.

ü Prepares timely pharmacovigilance reports for products and safety issues, including Individual Case Summary Reports (ICSRs) of Serious Adverse Events (SAEs), Annual IND reports, European Annual Safety Reports (ASRs), Development Safety Update Report (DSUR) Periodic Reports (PRs) line listings, and aggregate reports.

ü Begin to participate and demonstrate leadership on projects which enhance team and/or division performance. This includes acting as a lead contact for projects including global projects ensuring communication and process harmonization.

ü Work with Data Management or client on reconciliation of safety databases, if appropriate.

ü Monitor workflow for assigned studies/programs to ensure all deadlines are met.

ü Draft/modify and deliver safety presentations

o   Serious Adverse Event reporting at Investigator meetings

o   Client capabilities meetings, as appropriate

o   “Department Overview” to internal clients

ü Maintains a comprehensive understanding of Covance PV&DSS’ Standard Operating Procedures (SOPs), Work Instructions (WI), guidance documents and directives associated with safety management, reporting and pharmacovigilance.

ü Possess knowledge of other procedural documents, e.g. SOPs, etc. that impact PV&DSS.

ü Assist in the development of departmental Work Instructions (WI) and Standard Operating Procedures (SOPs), as appropriate.

ü Ensure compliant safety reporting in accordance with US and international reporting regulations, SOPs and safety processing guidelines set forth by departmental management team and the client.

ü Participate in the generation of monthly status and other project-specific reports ensuring the quality and accuracy of metrics/data are provided.

ü Support/train less experienced safety staff in all aspects of case-handling, adverse event reporting and other work, as needed.

ü Build and maintain good PV&DSS relationships across functional units.

ü Demonstrate role-specific Competencies on a consistent basis.

ü Demonstrate company Values on a consistent basis.

ü Begin to prepare Safety Management Plans (SMPs), Reconciliation Plans and other safety-specific plans under supervision.

ü Responsible for making decisions regarding adverse event reporting within the guidelines of each specific project.

ü Assist PV&DSS management to identify out of scope work.

ü Actively participates in project team and client meetings and liaise with clients, where appropriate.

ü Prepare and/or participate in client or regulatory audits.

ü Assist in the review of cumulative safety data for submission to Drug Safety Monitoring Boards (DSMBs), regulatory authorities or clients.

ü Assist with the set-up of, and the provision of data to Safety Committees/DSMBs.

ü Assist in the co-ordination of endpoint committees, as required.

ü Any other duties as assigned by management.

Education/Qualifications

ü Non-degree + 5-6 yrs safety experience*

ü Associate degree + 4-5 yrs safety experience*

ü Associate degree RN + 4-5 yrs safety experience*

ü BS/BA + 3-4 yrs safety experience*

ü MS/MA + 2-3 yrs relevant experience** (1-2 yrs safety experience)

ü Pharm D + 1-2 yrs relevant experience** (1 yr safety experience)

For Pharm D, a one year residency of fellowship can be considered relevant experience.

Degree preferred to be in one or more of the following disciplines: Biological Sciences, Pharmacy, Nursing, Life Sciences, and Chemistry.

*Safety experience includes actual experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions.

**Relevant experience includes experience in the pharmaceutical, biotechnology, or CRO industry, partly in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Data Monitor, Regulatory Affairs, or Quality Assurance.

Experience

o   Good verbal, written and presentation skills.

o   Good communication.

o Ability to interact and influence with line and middle management, staff and external contacts on a functional and tactical level.

o   High degree of accuracy with attention to detail.

o   Functions as a team player.

o   Ability to present and share useful business information across departments and functions.

o   Ability to anticipate and identify problems and take appropriate action to correct.

o   Knowledge of medical and drug terminology

o   Knowledge of Good Clinical Practice (GCP) related to clinical safety documentation

o   Knowledge of ICH Guidelines

o   Knowledge of Medical Device reporting desirable

o   Knowledge of worldwide regulatory requirements and reporting of adverse event for both marketed and investigational products.

o Good knowledge and understanding of industry and R&D processes and objectives.

o  Ability to work independently with minimal supervision

o  Good keyboard skills, preferably with knowledge of MS office and Windows would be beneficial.

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