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25 days old

Clinical Protocol Development Consultant

Kelly Services
Boston, MA 02133
Kelly Scientific has a new opening for a Clinical Protocol Development Consultant with a Global Pharmaceutical company in Downtown Boston. If you are an experienced Clinical Scientist with an Oncology and Hematology focus developing and implementing clinical protocols and documents, we would love to help move you forward in the process!



**Day-to-Day Responsibilities:**




+ This position reports to the Sr Director/VP of Clinical Development

+ Serve as Clinical Science Lead of Oncology for the Clinical Research and Development team

+ Lead the design and data collection of clinical drug programs to determine the efficacy based on trial results

+ Lead the Clinical Development Plan which will include but is not limited to: authoring clinical protocols, amendments, safety monitoring plans, scientific manuscripts, scientific presentations, IND reports, clinical study reports, and investigator brochures

+ Generate Clinical data to ensure the drug program objectives are being met by monitoring, evaluating, analyzing, and presenting scientific and medical data

+ Act as liaison with external panels such as the Data Safety Monitoring Board and Steering Committees

+ Perform medical literature and technology reviews in order to improve clinical protocol developments

+ Collaborate with Medical Directors, Clinical Operations, and various R&D organizations for clinical reviews of data

+ Develop and implement Data Quality Plan while tracking, analyzing, and reporting safety-related guidelines and documentation

+ Impact Clinical Development by staying current on scientific developments, trends, and innovative practices



**You are an excellent candidate if you meet the following requirements:**




+ Minimum of Bachelors Degree in Life Sciences Discipline, **required**

+ **Preference given** for MS/PhD/PharmD in Life Sciences Discipline

+ Lead Clinical Scientist Role 4-7 years Pharmaceutical Industry experience with a focus in Phase I III Oncology Clinical Drug Development, **required**

+ Clinical Manager Role - 7-10+ years of Pharmaceutical Industry Management experience with a focus in Phase I III Oncology Clinical Drug Development, **required**

+ Hematology expertise, **given preference**

+ Extensive experience in Clinical Trial Design and Management with hands-on experience developing, authoring, implementing, and reviewing essential documents such as, but not limited to, clinical trial protocols and protocol amendments

+ Expertise in Medical Oncology drug discovery technologies and patient care advancements in order to serve as a liaison with Clinical Investigators, Medical Directors, and Executive Leadership

+ Demonstrated ability to present clinical data and complex findings to team members, Senior Management, and External influencers

+ Ability to travel ~20% of the time, once COVID restrictions are lifted



Hourly rate will range between $82.00 - $110.00/hr. and will commensurate with background and related experience. Core hours are Monday Friday from 10:00am 3:00pm with flexibility before and/or after in order to support International partners. Remote work is an option. There is the potential for a permanent hire, eligible for a 15% annual bonus and relocation assistance.



Please apply online today! The right candidate will start in December.




**Why Kelly** **** **?**



Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interestsits the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.




**About Kelly** ****



At Kelly, were always thinking about whats next and advising job seekers on new ways of working to reach their full potential. In fact, were a leading advocate for temporary/non-traditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live. Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.


Kelly is an equal opportunity employer committed to employing a diverse workforce and providing accommodations for people with disabilities in all parts of the hiring process as required under its Employment Accommodation Policy. Kelly will work with applicants to meet accommodation needs that are made known to Kelly in advance.

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Posted: 2020-11-06 Expires: 2020-12-07

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Clinical Protocol Development Consultant

Kelly Services
Boston, MA 02133

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