BioSpace
Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing
BioSpace, North Chicago, Illinois, us, 60086
Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing
Join to apply for the Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing role at BioSpace.
Responsibilities
Prepare scientific reports and presentations related to clinical trials using available software and templates.
Assist in constructing phase 1 clinical study planning documents, and write Phase 1 protocols.
Review clinical protocols and key decisions impacting project timelines with management.
Comply with procedures set forth in relevant IQS documents and study protocols, and other directives issued by management regarding clinical/preclinical studies.
Apply experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded efficacy and safety reviews and ensure the scientific integrity of all processes.
Responsible for receiving and completing tasks and assignments from Therapeutic Area MD or Scientific Staff within timelines with minimal supervision.
Ensure scientific integrity of all processes by applying current electronic document conventions and processes consistently and accurately.
Integrate clinical trial data across studies and identify issues impacting projects and provide this information to internal peers and therapeutic area management.
Perform literature/competitive intelligence searches to recognize/resolve scientific and technical problems by applying the most current electronic document conventions and processes consistently and accurately.
Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management.
Responsible for maximizing individual, therapeutic area and team productivity; and mentor therapeutic area personnel.
Qualifications
Bachelor's/Master's degree in a science-related field with +7 years experience in the pharmaceutical industry.
Understanding of clinical study principles.
Good oral and written communication skills.
Proficiency in using computers to analyze clinical study data, generate reports and create presentations, posters, and manuscripts.
Knowledge of complex scientific analyses, business-related procedures, and project leadership.
Experience supporting clinical research, drug development and/or therapeutic area operations.
Proven record of successful projects.
Ability to produce work of the highest quality by paying attention to detail.
Ability to appropriately and effectively use resources to complete tasks and meet required timelines.
Independent expertise/experience to analyze clinical study/statistical data using available software.
Benefits and Additional Information This is a hybrid opportunity that requires being onsite 3x/week in the Lake County, IL office.
The compensation range described below is the range of possible base pay compensation that the company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer / Veterans / Disabled.
US & Puerto Rico only – to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html.
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html.
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Responsibilities
Prepare scientific reports and presentations related to clinical trials using available software and templates.
Assist in constructing phase 1 clinical study planning documents, and write Phase 1 protocols.
Review clinical protocols and key decisions impacting project timelines with management.
Comply with procedures set forth in relevant IQS documents and study protocols, and other directives issued by management regarding clinical/preclinical studies.
Apply experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded efficacy and safety reviews and ensure the scientific integrity of all processes.
Responsible for receiving and completing tasks and assignments from Therapeutic Area MD or Scientific Staff within timelines with minimal supervision.
Ensure scientific integrity of all processes by applying current electronic document conventions and processes consistently and accurately.
Integrate clinical trial data across studies and identify issues impacting projects and provide this information to internal peers and therapeutic area management.
Perform literature/competitive intelligence searches to recognize/resolve scientific and technical problems by applying the most current electronic document conventions and processes consistently and accurately.
Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management.
Responsible for maximizing individual, therapeutic area and team productivity; and mentor therapeutic area personnel.
Qualifications
Bachelor's/Master's degree in a science-related field with +7 years experience in the pharmaceutical industry.
Understanding of clinical study principles.
Good oral and written communication skills.
Proficiency in using computers to analyze clinical study data, generate reports and create presentations, posters, and manuscripts.
Knowledge of complex scientific analyses, business-related procedures, and project leadership.
Experience supporting clinical research, drug development and/or therapeutic area operations.
Proven record of successful projects.
Ability to produce work of the highest quality by paying attention to detail.
Ability to appropriately and effectively use resources to complete tasks and meet required timelines.
Independent expertise/experience to analyze clinical study/statistical data using available software.
Benefits and Additional Information This is a hybrid opportunity that requires being onsite 3x/week in the Lake County, IL office.
The compensation range described below is the range of possible base pay compensation that the company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer / Veterans / Disabled.
US & Puerto Rico only – to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html.
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html.
#J-18808-Ljbffr