Require Senior Clinical Research Associate at IQVIA @ Apply Now

Post : Sr Clin Process Assoc

Job Description 
Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. With a relentless focus on quality and innovation, Q2 Solutions uses its global experience and scientific expertise to transform science and data into actionable medical insights that help customers improve human health. A joint venture of IQVIA (formerly QuintilesIMS) and Quest Diagnostics, Q2 Solutions combines the best of each parent organization’s clinical trials laboratory services capabilities to fulfill its mission of treating each sample as if a life depends on it.

Responsibilities
1) On time completion of assigned role specific trainings (self-learning courses, instructor led training, acknowledgement of e-SOP/WI etc.) and related assessment
2) Under no to minimal supervision perform centralized monitoring activities for the assigned projects which includes but is not limited to:
a. Loading and maintaining the working databases with details of participating sites  
b. Coordinating for needful accesses for the site, clinical and project management teams
c. Ensuring on-time completion of documentation(s) that form a part of the regulatory dossier for kit and sample shipment
d. Ensuring on-time release of correct, complete and accurate patient laboratory report by following up on the associated pending activity(ies) and related team(s)
e. Ensuring that documentation is available for all activities performed for real-time audit readiness
f. Participation in departments initiatives/drives as applicable

Candidate Profile
• Minimum bachelor’s degree in life sciences/ pharmacy/allied fields
• Basic knowledge of applicable research and regulatory requirements, i.e., ICH GCP and relevant local laws, regulations and guidelines
• Excellent skills in MS Applications (Microsoft Word, Excel and PowerPoint)
• Excellent analytical skills
• Excellent verbal and written communication skills
• Excellent data entry skills
• 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.

Additional Information 
Qualification : B.Pharm, B.Sc
Location : Thane
Industry Type : Pharma
End Date : 20th May, 2019

Require Consultant at IQVIA @ Click Here for more details

Post : Consultant

Job Description
Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

Candidate Profile
• Graduation in Life Sciences/Pharma related subject + Master’s Degree (MBA) or M. Pharm
• 5-7 years of experience in pharmaceuticals primary market research analysis and consulting role
• Experience in primary market research with a focus on QUALITATIVE research, discussion guide design, content analysis, story-boarding, recommendation writing, client presentations
• Experience of managing clients/client facing role is essential
• Excellent English reading and written skills; excellent communication and interpersonal skills

Additional Information 
Qualification : Graduation in Life Sciences, MBA, M.Pharm
Experience: 5-7 year
Location : Bangalore, India
Industry Type : Pharma
End Date : 10th May, 2019

IQVIA hiring Gradutes @ Apply Now

Require Clinical Process Coordinator Process Coord at IQVIA @ Apply Now

Post : Clinical Process Coordinator

Job Description 
Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. With a relentless focus on quality and innovation, Q2 Solutions uses its global experience and scientific expertise to transform science and data into actionable medical insights that help customers improve human health.  A joint venture of IQVIA (formerly QuintilesIMS) and Quest Diagnostics, Q2 Solutions combines the best of each parent organization’s clinical trials laboratory services capabilities to fulfill its mission of treating each sample as if a life depends on it.

RESPONSIBILITIES
1) On time completion of assigned role specific trainings (self-learning courses, instructor led training, acknowledgement of e-SOP/WI etc.) and related assessment
2) Under no to minimal supervision perform centralized monitoring activities for the assigned projects which includes but is not limited to:
a. Loading and maintaining the working databases with details of participating sites 
b. Coordinating for needful accesses for the site, clinical and project management teams
c. Ensuring on-time completion of documentation(s) that form a part of the regulatory dossier for kit and sample shipment
d. Ensuring on-time release of correct, complete and accurate patient laboratory report by following up on the associated pending activity(ies) and related team(s)
e. Ensuring that documentation is available for all activities performed for real-time audit readiness
f. Participation in departments initiatives/drives as applicable

Candidate Profile
• Minimum bachelor’s degree in life sciences/ pharmacy/allied fields.
• 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.
• Basic knowledge of applicable research and regulatory requirements, i.e., ICH GCP and relevant local laws, regulations and guidelines
• Excellent skills in MS Applications (Microsoft Word, Excel and Power Point)
• Excellent analytical skills
• Excellent verbal and written communication skills
• Excellent data entry skills

Additional Information 
Qualification : B.Pharm, B.Sc
Location : Bangalore
Industry Type : Pharma
End Date : 30th March, 2019

Walk in Interview 20-23 Feb @ IQVIA

Walk in Interview at IQVIA @ 2 Feb 2019

Appl for Clinical Data Coder at IQVIA @Click here for more details

Quintiles and IMS Health have come together to become IQVIA, The Human Data Science Company. Inspired by the industry we help, IQVIA commits to providing solutions that enable life sciences companies to innovate with confidence, maximize their opportunities and ultimately drive human health outcomes forward.

Post : Clin Data Coder 1

Job Description
PURPOSE 
Provide basic and some comprehensive data management expertise (defined as efficient and quality data management products) to Data Management (DM) team to meet sponsor and company needs. Perform Clinical Data Management and/or Coding activities, and may also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager.

RESPONSIBILITIES
• Serve independently as a Clinical Data Coder (Coder) or in a leadership role in a specific DM area (e.g. Lead Coder) or DOC for one or more protocols with less than 5 operations staff, with guidance.
• Perform Medical Coding using MedDRA, WHO Drug and/or other relevant dictionaries as applicable.
• Validates/tests the coding set up and programming of coding reports; may also test databases, edit specifications or any related programming activities.
• May serve in the role of back-up to a lead coder.
• Conduct data review.
• Write and resolve data clarifications.
• May perform Serious Adverse Event (SAE) reconciliation activities.
• Understand and comply with core operating procedures and work instructions.
• Perform other duties as directed by the Lead Coder, DOC, DTL or Manager.
• Meet objectives as assigned.
• Develop and maintain good communications and working relationships with the DM team.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
• Thorough knowledge of Medical Terminology.
• Thorough knowledge of Medical Dictionaries used for coding (e.g. MedDRA, WHODD etc.).
• Excellent organizational, communication and leadership skills.
• Ability to exercise excellent attention to detail and act independently with the initiative required to resolve problems.
• Basic understanding of database technologies related to data management and coding.
• Ability to work on computer systems with ease and good working knowledge of computer programs.
• Excellent English written and oral communication skills.
• Knowledge of operating procedures and work instructions and the ability to apply them in practice.
• Able to present information effectively to individuals and small groups.
• Basic understanding of Drug Development Process and its relevance to Data Management.
• Ability to establish and maintain effective working relationships with co-workers, managers and clients.

Candidate Profile
• Bachelor’s degree or educational equivalence in pharmacy, life sciences or related field or medical, nursing qualification with 1 year relevant experience or equivalent combination of education, training and experience.
• Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
• Extensive use of keyboard requiring repetitive motion of fingers.
• Extensive need to view computer screen for extended periods of time.

Additional Information 
Qualification : B.Pharm, B.Sc
Experience: 1 year
Location : Bangalore
Industry Type : Pharma
End Date : 10th January, 2019

Require Associate Manager in Safety Operations at IQVIA

IQVIA  is The Human Data Science Company focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

Post : Associate Manager, Safety Operations

Job Description

• Implement and support operational decisions as determined and instructed by senior management. May contribute and assist in global initiatives e.g. Change Management; Subject Matter Expert (SME) Committees; SOP Review Committees; Retention, Engagement, training, processes etc.
• Assist in the implementation for measuring and improving employee engagement local and/or global actions. Maintain open and regular communication with direct reports to ensure a supportive working environment.
• Supervise SO staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work; performance appraisal and professional development guidance; rewarding and disciplining employees; addressing employee relations issues; resolving problems and absence management. Approve actions on human resources matters.
• Support the management of project resource assignments staff hiring and staff terminations in collaborations with operations specialist managers. Assists with staff training; professional and career development.
• Work closely with operations managers to address problem areas, work scheduling for current and projected projects, and projected peak workloads. Monitor, assess and report utilization of staff. Identify and implement solutions to address poor utilization.
• Ensure direct reports are cross trained on Lifecycle Safety service offering; monitor and develop training plans; identify training and development needs of staff in collaboration with Lifecycle Safety Infrastructure group and Lifecyle Safety Management (LSM).
• Lead and encourage direct reports in continuous improvement of department work processes, procedures and infrastructure. Instruct and lead direct reports in efficient management of project budgets through effective timesheet reporting. Work closely with operations specialist managers.
• Monitor and ensure that project processes and department deliverables meet expected quality, financial and productivity targets. Assist with meeting department utilization and realization targets.
• Ensure timely movement of project work through the process steps, in accordance with governing SOPs, ICH/FDA regulations and guidelines, working instructions and client expectations.
• Ensure that staff have been trained on and are following required Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), FDA and ICH guidelines and regulations, Working Instructions and project instructions.
• Work with LSM constructively in a matrix framework to achieve project and customer deliverables.
• Perform other duties as assigned

Candidate Profile
Bachelor's degree or educational equivalent in health science or other directly related field and 5 years' clinical research experience in a Contract Research Organization or Pharmaceutical company including at least 3 years of Lifecycle Safety experience(Pharmacovigilance, CEVA, Medical Information, Safety Publishing, Risk Management, etc.) or equivalent combination of education, training or experience.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Sound knowledge of Lifecycle Safety service lines; willingness to increase knowledge across Lifecycle Safety service lines and develop new skills.
• Staff management skills, effective leadership, motivational and influencing skills.
• Ability to work on multiple projects and manage competing priorities.
• Ability to mentor and coach.
• Strong presentation, report writing skills and customer focus skills.
• Ability to achieve results through communication and facilitation in a matrix service delivery environment with shared accountabilities.
• Sound judgment, decision-making and problem solving skills.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.

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.
• Requires occasional travel.

Additional Information :
Experience : 3-5 years
Qualification : Bachelor's degree
Location : Bangalore
Industry Type : Pharma
Functional Area : Safety Operations
End Date : 20th November, 2018

Require Associate Manager in Safety Operations at IQVIA @Apply Now

IQVIA  is The Human Data Science Company focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

Post : Associate Manager, Safety Operations

Job Description

• Implement and support operational decisions as determined and instructed by senior management. May contribute and assist in global initiatives e.g. Change Management; Subject Matter Expert (SME) Committees; SOP Review Committees; Retention, Engagement, training, processes etc.
• Assist in the implementation for measuring and improving employee engagement local and/or global actions. Maintain open and regular communication with direct reports to ensure a supportive working environment.
• Supervise SO staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work; performance appraisal and professional development guidance; rewarding and disciplining employees; addressing employee relations issues; resolving problems and absence management. Approve actions on human resources matters.
• Support the management of project resource assignments staff hiring and staff terminations in collaborations with operations specialist managers. Assists with staff training; professional and career development.
• Work closely with operations managers to address problem areas, work scheduling for current and projected projects, and projected peak workloads. Monitor, assess and report utilization of staff. Identify and implement solutions to address poor utilization.
• Ensure direct reports are cross trained on Lifecycle Safety service offering; monitor and develop training plans; identify training and development needs of staff in collaboration with Lifecycle Safety Infrastructure group and Lifecyle Safety Management (LSM).
• Lead and encourage direct reports in continuous improvement of department work processes, procedures and infrastructure. Instruct and lead direct reports in efficient management of project budgets through effective timesheet reporting. Work closely with operations specialist managers.
• Monitor and ensure that project processes and department deliverables meet expected quality, financial and productivity targets. Assist with meeting department utilization and realization targets.
• Ensure timely movement of project work through the process steps, in accordance with governing SOPs, ICH/FDA regulations and guidelines, working instructions and client expectations.
• Ensure that staff have been trained on and are following required Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), FDA and ICH guidelines and regulations, Working Instructions and project instructions.
• Work with LSM constructively in a matrix framework to achieve project and customer deliverables.
• Perform other duties as assigned.

Candidate Profile
Bachelor's degree or educational equivalent in health science or other directly related field and 5 years' clinical research experience in a Contract Research Organization or Pharmaceutical company including at least 3 years of Lifecycle Safety experience(Pharmacovigilance, CEVA, Medical Information, Safety Publishing, Risk Management, etc.) or equivalent combination of education, training or experience.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Sound knowledge of Lifecycle Safety service lines; willingness to increase knowledge across Lifecycle Safety service lines and develop new skills.
• Staff management skills, effective leadership, motivational and influencing skills.
• Ability to work on multiple projects and manage competing priorities.
• Ability to mentor and coach.
• Strong presentation, report writing skills and customer focus skills.
• Ability to achieve results through communication and facilitation in a matrix service delivery environment with shared accountabilities.

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.
• Requires occasional travel.

Additional Information :
Experience : 3-5 years
Qualification : Bachelor's degree
Location : Bangalore
Industry Type : Pharma
Functional Area : Safety Operations
End Date : 20th November, 2018

IQVIA require Consultant @ Apply Now

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

Post : Consultant

Job Description 
Clinical coding and clinical support for site identification and optimization

Responsibilities:
• Identify right set of ICD diagnosis and procedure codes/NDC based on trial protocol
• Identify/rank clinical sites based on research on drug usage - posology
• conversion of data to patient equivalents and DoT
• Desk research on epidemiology
• Identify potential clinical investigators based PUBMED analytics/social media/patient load/conferences

ssociate Manager in Safety Operations at IQVIA

Post : Associate Manager, Safety Operations

Job Description

• Implement and support operational decisions as determined and instructed by senior management. May contribute and assist in global initiatives e.g. Change Management; Subject Matter Expert (SME) Committees; SOP Review Committees; Retention, Engagement, training, processes etc.
• Assist in the implementation for measuring and improving employee engagement local and/or global actions. Maintain open and regular communication with direct reports to ensure a supportive working environment.
• Supervise SO staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work; performance appraisal and professional development guidance; rewarding and disciplining employees; addressing employee relations issues; resolving problems and absence management. Approve actions on human resources matters.

Require Senior Clinical Data Coder at IQVIA

Senior Clinical Data Coder-1806505

Join us on our exciting journey!
IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
• Excellent knowledge of Medical Terminology, Pharmacology, Anatomy, or Physiology required for many tasks.
• Thorough knowledge of Medical Dictionaries used for coding (e.g. MedDRA, WHODD etc.).

Require Associate Manager in Operations Team at IQVIA

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

Post : Assoc Mgr, Operations Team - (R1027277)