Project Manager

Job Opening for Project Manager- Pharma, Kankakee, IL

We are currently working on below mentioned i., e. Job Opening for Project Manager- Pharma, Kankakee, IL. Please let me know if you are interested in applying for the same.

8-10 yrs. exp., but fewer is ok depending on background
Pharma Industry experience not required
PMP a plus
6mos – 1yr assignment

Job Description:  Note this is a generic JD from the client, but not all are required.
Applies GMP/GLP in all areas of responsibility, as appropriate
Represents the single point of control for research studies and projects
Coordinates efforts of the study team
Manages client relationships
Compiles and communicates study requirements to appropriate study team members
Develops protocols and ensures that the protocol and report, including any changes, are approved and in compliance with appropriate SOPs, GXPs, quality agreements, and regulatory agency guidelines
Provides relevant information to assure accuracy of forecast and revenue recognition, reviews cost estimate and financial information for accuracy
Monitors progress and status of assigned studies.  Ensures that all experimental data, including observations of unanticipated responses to the test system, are accurately recorded, and verified
Leads efforts with the study team to troubleshoot and solve assay problems, as necessary
Reviews reports for scientific accuracy and completeness
Provides technical/scientific guidance and leadership to ensure project completion and to other areas of the company
Performs post-project analysis of study performance
Leads and sponsors client visits
Responsible for ensuring that any unforeseen circumstances that may affect the quality and integrity of the study are identified and documented as they occur and corrective action is taken
Responds to unscheduled deadlines, client needs, and crises without neglecting other duties
Co-authors scientific papers/posters which are published or presented at scientific meetings
Assures on-time delivery of high-quality data and reports
Evaluates data to assure regulatory guidelines and scientific expectations are met
On a broad basis, able to apply appropriate chemistry principles, theories, and concepts within the field of discipline.  Applies a working knowledge of related disciplines
Trains less-experienced staff
Performs other related duties as assigned
Travels to various EFII and client locations to support studies and projects
Travels to technical conferences to represent Eurofins
Conducts all activities in a safe and efficient manner
Performs other duties as assigned

Project manager is responsible for ensuring that drugs are developed on time, within budget and in line with all scientific requirements for safety and efficacy. Their day-to-day responsibilities may include:

Managing key projects, stakeholders, and personnel, such as biochemical engineers, researchers, scientists, healthcare consultants and physicians.
Establishing and maintaining timelines for drug trials and ensuring proper, compliant completion of each one.
Staying up to date on all applicable regulatory guidelines, like rules from the U.S. Food and Drug Administration.
Keeping detailed records on the progress of research, trials, and approvals from one phase to the next, in accordance with regulatory mandates and corporate governance rules.
Evaluating the results of trials and in appropriate cases choosing to halt development due to safety concerns, inefficacy, or side effects

Job Opening for Project Manager- Pharma, Kankakee, IL

We are currently working on below mentioned i., e. Job Opening for Project Manager- Pharma, Kankakee, IL. Please let me know if you are interested in applying for the same.

8-10 yrs. exp., but fewer is ok depending on background
Pharma Industry experience not required
PMP a plus
6mos – 1yr assignment

Job Description:  Note this is a generic JD from the client, but not all are required.
Applies GMP/GLP in all areas of responsibility, as appropriate
Represents the single point of control for research studies and projects
Coordinates efforts of the study team
Manages client relationships
Compiles and communicates study requirements to appropriate study team members
Develops protocols and ensures that the protocol and report, including any changes, are approved and in compliance with appropriate SOPs, GXPs, quality agreements, and regulatory agency guidelines
Provides relevant information to assure accuracy of forecast and revenue recognition, reviews cost estimate and financial information for accuracy
Monitors progress and status of assigned studies.  Ensures that all experimental data, including observations of unanticipated responses to the test system, are accurately recorded, and verified
Leads efforts with the study team to troubleshoot and solve assay problems, as necessary
Reviews reports for scientific accuracy and completeness
Provides technical/scientific guidance and leadership to ensure project completion and to other areas of the company
Performs post-project analysis of study performance
Leads and sponsors client visits
Responsible for ensuring that any unforeseen circumstances that may affect the quality and integrity of the study are identified and documented as they occur and corrective action is taken
Responds to unscheduled deadlines, client needs, and crises without neglecting other duties
Co-authors scientific papers/posters which are published or presented at scientific meetings
Assures on-time delivery of high-quality data and reports
Evaluates data to assure regulatory guidelines and scientific expectations are met
On a broad basis, able to apply appropriate chemistry principles, theories, and concepts within the field of discipline.  Applies a working knowledge of related disciplines
Trains less-experienced staff
Performs other related duties as assigned
Travels to various EFII and client locations to support studies and projects
Travels to technical conferences to represent Eurofins
Conducts all activities in a safe and efficient manner
Performs other duties as assigned

Project manager is responsible for ensuring that drugs are developed on time, within budget and in line with all scientific requirements for safety and efficacy. Their day-to-day responsibilities may include:

Managing key projects, stakeholders, and personnel, such as biochemical engineers, researchers, scientists, healthcare consultants and physicians.
Establishing and maintaining timelines for drug trials and ensuring proper, compliant completion of each one.
Staying up to date on all applicable regulatory guidelines, like rules from the U.S. Food and Drug Administration.
Keeping detailed records on the progress of research, trials, and approvals from one phase to the next, in accordance with regulatory mandates and corporate governance rules.
Evaluating the results of trials and in appropriate cases choosing to halt development due to safety concerns, inefficacy, or side effects