Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing

Job Title

Job Description

To build all necessary data/information needed in preparing internal documents/scientific reports related to clinical trials and; to keep multiple reports moving forward simultaneously through multi-tasking.

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.

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 the 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 timeline 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.

Bachelors/Master's degree, in Science related to Field with +7 years' experience in pharmaceutical industry

Understanding of clinical study principles

Must possess good oral and written communication skills

Must be proficient in using computer to analyze clinical study data, generate reports and create presentations, posters and manuscripts

Must have knowledge of complex scientific analyses, business-related procedures, and project leadership.

Experience supporting clinical research, drug development and/or therapeutic area operations.

Must have a 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 by using available software.

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.

Abb Vie 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

US & Puerto Rico applicants seeking a reasonable accommodation,  to learn more:

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Pay Range: $96500 - 183500 USD

Role is primarily site- or office-based but can occasionally be performed remotely. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays.

Three days in the office is the minimum; some individuals or teams may require more in-office days due to…