100% remote job - Clinical Research Scientist
100% remote job - Clinical Research Scientist
Cube Hub Inc.
California, United States
See who Cube Hub Inc. has hired for this role
Clinical Research Scientist
Job Location: Santa Monica, California (Remote Job)
Job Duration: 12 months
Acquires and utilizes knowledge of clinical trial design to develop specific study concept sheets and protocols.
Participates in protocol review discussions concerning scientific and procedural aspects of study design.
Prepares study protocols, amendments, specific sections of study manuals and Investigator meeting notebooks, and other documents as needed with appropriate guidance and supervision.
With supervision, contributes to the design and development of CRFs, Data Management Manuals and Data Analysis Plans.
With supervision, addresses questions regarding scientific and related procedural issues from Investigators.
With supervision, contributes to the preparation and/or review of data listings, summary tables, study results, manuscripts, and scientific presentations.
Assists in the preparation/review of regulatory documents, IND annual reports, IND safety reports, Investigator Brochures and NDAs.
Supports priorities within functional area.
Anticipates moderately complex obstacles within a clinical study and with guidance implements solutions.
May be asked to coordinate teams and provide direction.
May lead two or more specific components of departmental strategic initiatives.
Must be able to enter a new therapeutic area and summarize scientific information that is available in published literature to integrate into new study development.
Excellent verbal and written communication skills and interpersonal skills are required to maintain working relationship with team members to ensure scientific integrity of clinical studies.
May be sought out for advice by others within the company to help make better decisions and resolve moderately complex problems.
Job Location: Santa Monica, California (Remote Job)
Job Duration: 12 months
Acquires and utilizes knowledge of clinical trial design to develop specific study concept sheets and protocols.
Participates in protocol review discussions concerning scientific and procedural aspects of study design.
Prepares study protocols, amendments, specific sections of study manuals and Investigator meeting notebooks, and other documents as needed with appropriate guidance and supervision.
With supervision, contributes to the design and development of CRFs, Data Management Manuals and Data Analysis Plans.
With supervision, addresses questions regarding scientific and related procedural issues from Investigators.
With supervision, contributes to the preparation and/or review of data listings, summary tables, study results, manuscripts, and scientific presentations.
Assists in the preparation/review of regulatory documents, IND annual reports, IND safety reports, Investigator Brochures and NDAs.
Supports priorities within functional area.
Anticipates moderately complex obstacles within a clinical study and with guidance implements solutions.
May be asked to coordinate teams and provide direction.
May lead two or more specific components of departmental strategic initiatives.
Must be able to enter a new therapeutic area and summarize scientific information that is available in published literature to integrate into new study development.
Excellent verbal and written communication skills and interpersonal skills are required to maintain working relationship with team members to ensure scientific integrity of clinical studies.
May be sought out for advice by others within the company to help make better decisions and resolve moderately complex problems.
-
Seniority level
Mid-Senior level -
Employment type
Contract -
Job function
Research, Analyst, and Information Technology -
Industries
Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Cube Hub Inc. by 2x
See who you knowGet notified about new Clinical Research Scientist jobs in California, United States.
Sign in to create job alertSimilar jobs
People also viewed
-
Hiring Clinical Scientist - Entry at Santa Rosa, CA for Abbott
Hiring Clinical Scientist - Entry at Santa Rosa, CA for Abbott
-
Scientist, Antibody Engineering
Scientist, Antibody Engineering
-
AD, Clinical Scientist (Office or Remote)
AD, Clinical Scientist (Office or Remote)
-
Clinical Scientist at Temecula, CA
Clinical Scientist at Temecula, CA
-
Research and Development Scientist
Research and Development Scientist
-
Scientist I
Scientist I
-
Looking for Clinical Scientist - CA
Looking for Clinical Scientist - CA
-
Clinical Scientist
Clinical Scientist
-
Senior Pharmacovigilance Scientist
Senior Pharmacovigilance Scientist
Similar Searches
Explore collaborative articles
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
Explore More