Associate I, Clinical Pharmacology Scientific Support & Reporting

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

Benefits offered by this job

Paid time off

Insurance (medical/dental/vision)

401(k) plan

Job summary

You will perform literature searches and pharmacokinetic analyses, collaborating with Scientists and Therapists. This role emphasizes accuracy, timely delivery, and opportunities for process improvement.

Qualifications

• Bachelor’s degree in Science or related field with 2+ years in pharma; Master’s in pharmacology or related field preferred.
• Associate degree / RN with 6+ years in pharma may be considered.
• Must possess strong 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 for clinical trials using available software and templates.
• Assist in constructing phase 1 study planning documents and write Phase 1 protocols.
• Comply with IQS procedures and study protocols.
• Follow directives from management regarding clinical studies.
• Strive to produce high-quality work.
• Perform literature and competitive intelligence searches.
• Analyze clinical study data using software for pharmacokinetic analysis.
• Receive and complete tasks from Scientific Staff or Therapeutic Area MD within deadlines.

Skills

Oral & written communication

Report generation

Data analysis

Presentation creation

Quality focus

Education

Bachelor’s degree in Science or related field

Master’s degree in pharmacology or related field

Associate degree / RN with 6+ years in pharma

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 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 determinate. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employer 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.