Clinical Pharmacology Data & Reporting Associate

AbbVie Inc.; Chicago (IL); Hybrid; USD 70,000 - 95,000; Full time

Benefits offered by this job

Short-term incentive programs

Comprehensive benefits package

401(k) plan

Job summary

AbbVie in Chicago seeks a Scientific Reports Associate to support internal clinical trial documentation, assist blinded efficacy and safety reviews, and prepare reports using standard templates. You will help draft Phase 1 study planning documents and Phase 1 protocols, ensuring compliance with IQS and directives from management.

Qualifications include a Bachelor's in Science with 2+ years in pharma, or an Associate/RN with 6+ years.

Qualifications

• Must possess good oral and written communication skills.
• Ability to use computer to generate reports, analyze data, and create presentations.
• Previous experience may be narrowly-focused or limited.
• Ability to identify opportunities and participate in process improvement initiatives.

Responsibilities

• Prepare scientific reports and presentations related to clinical trials using templates.
• Assist in constructing phase 1 study planning documents and write Phase 1 protocols.
• Comply with IQS documents and study protocols.
• Follow directives issued by management regarding clinical studies.
• Commit to producing work of the highest quality and accuracy.
• Pay close attention to detail in all deliverables.
• Perform literature and competitive intelligence searches.
• Analyze clinical study data with software to support blinded/un-blinded PK analyses.

Skills

Oral and written communication

Data analysis

Presentation creation

Pharmacology understanding

Education

Bachelor's degree in Science

Master's degree in pharmacology

Associates degree / RN

Job description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.

Job Description

To build all necessary data/information needed to prepare internal documents/scientific reports related to clinical trials by assisting with ongoing blinded efficacy and safety reviews.

Responsibilities

• Prepare scientific reports and presentations related to clinical trials using available software and templates.
• Assists in constructing phase 1 clinical study planning documents, and writes Phase 1 protocols.
• Comply with procedures set forth in relevant IQS documents and Study protocols
• Comply with the directives issued by the management regarding clinical studies.
• Commit to producing work of the highest quality
• Pay close attention to detail
• Perform literature and competitive intelligence searches
• Apply experience to analyze clinical study data, using available software to assist with ongoing blinded/un-blinded pharmacokinetic analysis
• Responsible for receiving and completing assignments and tasks from functional Scientific Staff or Therapeutic Area MD within a given time period with supervision.

Qualifications

• Bachelor’s degree, in Science, related to Field with +2 years’ experience in pharmaceutical industry. Or Masters degree in pharmacology or related field.
• Associates degree/RN with 6+ years of experience in pharmaceutical industry may be additionally considered.
• Must possess good oral and written communication skills
• Ability to use computer to generate reports, analyze data, and create presentations
  
• Previous experience may be narrowly-focused or limited.
• Ability to identify opportunities and participate in process improvement initiatives.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at thetimeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographiclocation,andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
• This job is eligible toparticipatein our short-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable law.

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, visithttps://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