US
0 suggestions are available, use up and down arrow to navigate them
PROCESSING APPLICATION
Hold tight! We’re comparing your resume to the job requirements…
ARE YOU SURE YOU WANT TO APPLY TO THIS JOB?
Based on your Resume, it doesn't look like you meet the requirements from the employer. You can still apply if you think you’re a fit.
Job Requirements of Clinical Scientist:
-
Employment Type:
Contractor
-
Location:
Cambridge, MA (Onsite)
Do you meet the requirements for this job?
Clinical Scientist
Careers Integrated Resources Inc
Cambridge, MA (Onsite)
Contractor
Job Title: Clinical Scientist
Location: Cambridge, MA(Onsite)
Duration: 6 Months+
Shift: 1st Shift
Duties:
Education:
Masters, PhD, or PharmD in related field
Skills:
Allergy, Hematology, Oncology experience in a clinical setting
Languages:
English(Speak, Read, Write )
Location: Cambridge, MA(Onsite)
Duration: 6 Months+
Shift: 1st Shift
Duties:
- Work on our Systemic Mastocytosis portfolio as well as BLU 808 trial.
- Work closely with Medical Directors, Pharmacology, Discovery, external experts, and investigators to accumulate scientific and medical knowledge necessary to support clinical development plans and study designs and protocols.
- Assist Medical Directors in creation of proposed concept sheets for clinical studies and may write protocols and informed consent documents through incorporation of input from both internal and external experts.
- Assist with the annual update of IB with input from Toxicology, Pharmacology, Safety, Regulatory Drive and integrates clinical contribution to answering regulatory queries and other submissions related to studies.
- Monitor and review along with the medical monitor safety and efficacy data in ongoing studies; monitors GCP compliance with help of clinical operations and CRO.
- Involved in high level data cleaning activities requiring clinical judgment Involved in analysis of complex data for regulatory submissions, publications and design of studies and programs.
- Attending scientific meetings to remain abreast of new developments within relevant areas and to interact with investigators, and advisors.
- Work with investigative sites to answer protocol related questions, resolve study conduct and design issues.
- May present data, protocol designs and other information at advisory boards, investigator meetings, site initiations and other internal and external settings
Education:
Masters, PhD, or PharmD in related field
Skills:
Allergy, Hematology, Oncology experience in a clinical setting
Languages:
English(Speak, Read, Write )
Get job alerts by email.
Sign up now!
Join Our Talent Network!