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Clinical Scientist - part time

Kelly Services

Deerfield, IL
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Job Details

Job Title Clinical Scientist - part time

Jobid US33MXGR_BH1436055

Location: Deerfield, IL, 60015, USA

Description Kelly Services is seeking a part time **Clinical Scientist** for one of our leading clients in **Deerfield, IL** for a W2 contract opportunity.

Job Description: On-Site Deerfield

Part Time 10-20 hours week MAX.

Flex schedule 9 AM - 4 PM Mon- Fri

Highly desirable to have short notice availability to go into the office upon 24 hour advance notice.

Contract through end of 2018 possibly longer


Experience with clinical drug development preferably in the disease areas of inflammation, arthritis, gout, and/or metabolic diseases.

The Clinical Scientist will support the Medical Director during review and evaluation of scientific literature, internal study data and documents in preparation for internal team/management reviews and submissions to regulatory agencies.

This person will also support the Medical Director during preparation of presentation materials and may participate in team meetings during data and document reviews.


Clinical Development team participation and leadership- Represents Clinical Science on US/EU Development Supports the Global Development Team US, EU, Japan to ensure that the US/EU.

Development Team activities are aligned with the global strategy.- Responsible deliverables producing the Development Strategy, with significant contributions to assign sections of the Clinical Development Plan and Clinical Protocols.

Provides continual critical evaluation of the development strategy to maintain a state-of-the-art development plan that is competitive and consistent with the latest regulatory requirements, proactive identification of challenges, and development of contingency plans to meet them for those areas assigned.

Contributes to high impact global decisions: monitoring and interpreting data from ongoing internal and external studies and making recommendations that impact regional and global development such as go/no go decisions or modification of development plans or study designs that may have a significant impact on timelines or product labeling.

Synopsis / Protocol Development, Study Execution, Study Interpretation.

Assumes primary responsibility for the completion of protocol synopsis, obtaining scientific and corporate review committee approval including presentation and defense of the Synopses during review committee meetings, review and approval of documents related to study Protocols e.g. Statistical Analysis Plans and Safety Management Plans for assigned sections.

Provides scientific contributions and overall content approval of written responses required by IRB / Ethics Committees and critical study training meetings e.g. Investigator Meetings .

Responsible for review of study data, interpretation of results and communication of study conclusions within the company for assigned sections.

Trial Medical Monitoring- Manages collection of necessary information to assess issues relating to protocol conduct and/or individual subject safety.

Provides preliminary assessments to Medical Monitor for review and approval.

Reviews and assesses overall safety information in conjunction with Pharmacovigilance and Medical Monitor of record.External Interactions.

Successfully contributes to interactions with regulatory authorities / agencies and key opinion leaders relevant to assigned compound and participate in meetings with representatives of the regulatory organizations and the identification / contact / maintenance of strong Company relationships with key opinion leaders.

Influences establishment of strategy for the compound, and the development of documents required to outline the Company positions on research programs or regulatory applications e.g. briefing reports , materials used for meeting presentations, and formal responses to communications.

**If you meet the qualifications above and are interested in pursuing this opportunity, please submit your resume for immediate consideration!**

**Perks of being a Kelly employee:**

• Weekly electronic pay

• Access to more than 3,000 online training courses though Kelly Learning center

• Group rate insurance options available immediate upon hire*

• Service bonus plan and holiday pay*

• Online application system

• Never an applicant fee

*perks to be received upon meeting eligibility requirements

Important information: This position is recruited for by a remote Kelly office, not your local Kelly branch. To be considered for this position, you must use the Submit Resume or Apply Now button to submit your resume. If you have questions, the recruiter for this position can be reached via email at

**Why Kelly** **®** **?**

At KellyServices ® , we work with the best. Our clients include 95 of the Fortune100 ™ companies, and more than 70,000 hiring managers rely on Kelly annually to accessthe best talent to drive their business forward. If you only make one career connection today, connectwith Kelly.

**AboutKelly Services** **®**

As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 peoplearound the world and have a role in connecting thousands more with work through our global network oftalent suppliers and partners. Revenue in 2017 was $5.4 billion. Visit and connect with us on Facebook, LinkedIn and Twitter .

Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females,Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and iscommitted to employing a diverse workforce. Equal Employment Opportunityis The Law.

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