Associate I, Clinical Pharmacology Scientific Support & Reporting

ABBVIE; North Chicago (IL); On-site; USD 66,000 - 126,000; Full time

Job summary

AbbVie is seeking an Associate I in Clinical Pharmacology Scientific Support & Reporting in Illinois. You will prepare reports for clinical trials, assist with Phase 1 documents, and ensure compliance with study protocols and IQS guidelines.

The role requires 2+ years in pharma or a relevant Masters, strong communication, and data/reporting skills; opportunity to contribute to blinded/unblinded PK analyses and high-quality deliverables.

Qualifications

• Bachelor’s degree in Science with 2+ years in pharma, or a Masters in pharmacology.
• Associates degree/RN with 6+ years in pharma may be 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.

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 writes Phase 1 protocols.
• Comply with procedures in IQS documents and Study protocols.
• Comply with directives issued by management regarding clinical studies.
• Commit to producing work of the highest quality.
• Perform literature and competitive intelligence searches.
• Apply experience to analyze clinical study data, using software to assist with blinded/un-blinded pharmacokinetic analysis.
• Receive and complete assignments from Scientific Staff or Therapeutic Area MD within a given time period with supervision.

Skills

Communication skills

Data analysis

Report writing

Pharma experience

Education

Bachelor’s degree in Science

Masters in Pharmacology

Associates degree or RN with pharma experience

Tools

Pharmacokinetic software

Presentation software

Job description

Associate I, Clinical Pharmacology Scientific Support & Reporting

• Full-time
• Salary Min: 65500
• Salary Max: 125500
• Workday Global Grade: 14
• Compensation: USD 65,500 - USD 125,500 - yearly

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 at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

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
• 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.
• 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.

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’s sole and absolute discretion 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.

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