Associate I, Clinical Pharmacology Scientific Support & Reporting

BioSpace; North Chicago (IL); On-site; USD 70,000 - 110,000; Full time

Benefits offered by this job

Medical/dental/vision insurance

Paid time off

401(k) plan with company match

Short-term incentive programs

Job summary

AbbVie in the United States seeks a specialist to build data and information needed for internal clinical trial documents and scientific reports, supporting blinded efficacy and safety reviews.

You will prepare reports, assist in phase 1 study planning and protocols, ensure adherence to IQS and study directives, and contribute to high-quality output with meticulous attention to detail.

Qualifications

• Bachelor’s degree in Science or related field with 2+ years in pharma. Master’s in pharmacology or related field also acceptable.
• Associates degree/RN with 6+ years in pharma may be considered.
• Strong oral and written communication skills.
• Ability to generate reports, analyze data, and create presentations.
• 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 write Phase 1 protocols.
• Comply with IQS documents and Study protocols.
• Follow directives issued by management regarding clinical studies.
• Commit to producing high-quality work with attention to detail.
• Perform literature and competitive intelligence searches.
• Analyze clinical study data using software to assist with blinded/unblinded pharmacokinetic analysis.
• Receive and complete assignments from Scientific Staff within deadlines with supervision.

Skills

Oral and written communication

Data analysis

Report generation

Process improvement

Pharmaceutical industry experience

Education

Bachelor's degree in Science related field

Master's degree in pharmacology or related field

Associates degree / RN with 6+ years experience

Tools

MS Office Suite

Statistical software

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

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 or local law:

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.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable 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, 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