Job details
Job type full-time number of hires for this role 1
Qualifications
Bachelor`s (preferred)
Clinical trials: 1 year (preferred)
Clinical research: 1 year (preferred)
Full job description
Senior cra
Newave pharmaceutical inc (newave) is looking to hire a full-time senior cra in the us (remote city, work from home)Newave is a biotechnology company, located in pleasanton, ca, dedicated to the discovery and development of small molecule oral therapeutics to treat cancer, infection, and autoimmune diseases.
Description
Schedule: full-time
Work location:
**this is a work from home position and you can be located anywhere in the united states to be eligible for this roleEast coast or central us is preferred.
Responsibilities
Responsibilities primarily involve the management of assigned investigational study sites including pre-study, initiation, monitoring, and study close-out site visits.
Generate, revise, circulate and/or track project-specific documentation as needed including but not limited to the protocol, case report forms, and completion guidelines, informed consent forms, and regulatory packets.
Contribute to the maintenance of trial master file and electronic project organization and documentation system.
Maintain contact with study sites, sponsors, and other involved parties to ensure good communication and progress of the project.
Organize and/or participate in training exercises as needed to remain as current as possible in related areas.
Assist with writing, revising, and participate in training and presentations of industry standard operating procedures.
Qualification and requirements
Cra: 3 years (required): three or more years of work experience with clinical site monitoring experience for a cro / pharmaceutical company / biotechnology company
Experience in hematological malignancies phase i-iii clinical trials
Knowledge of good clinical practices (gcp), clinical monitoring, study site oversight and management, and regulatory compliance
Able to respond to issues/problem quickly and resolve them in timely manner.
Willing and able to travel
Excellent accuracy and attentiveness to detail
Enjoy the fast pace in start-up company
Strong written and verbal communication skills; strong interpersonal skills
Good organizational skills with the ability to multitask and prioritize workload
Good computer skills (word, excel, email)
Effectively work independently as well as within a team matrix, able to work with team members with various background and experiences
Ability to handle stressful situations and deadlines
Bachelor`s (required) (4 year program) or higher
We offer you an excellent total compensation package, including competitive salary, excellent benefit package and growth opportunitiesWe believe in our team and your ability to do excellent work with us.
Your benefits include 401k, pto, medical, dental and vision insuranceWe would love to talk to you about this fantastic opportunity.
Do you find this opportunity compelling? do you want to be part of something bigger than yourself? if so we encourage you to applyIf you are highly qualified you will hear from one of our recruitersWe are actively interviewing so apply today.
We are an equal opportunity employer and value diversity at our companyWe do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Notice
Our company’s recruiters are here to help unlock the next possibility within your career and we take your candidate experience very seriouslyDuring the recruitment process, no recruiter or employee will request financial or personal information (social security number, credit card or bank information, etc.) from you via emailThe recruiters will not email you from a public webmail client like gmail or yahoo mail.
Job type: full-time
Benefits:
401(k)
Dental insurance
Flexible spending account
Health insurance
Health savings account
Paid time off
Vision insurance
Schedule:
Monday to friday
Education:
Bachelor`s (preferred)
Experience:
Clinical trials: 1 year (preferred)
Clinical research: 1 year (preferred)
Work location:
Fully remote
Work remotely:
Yes
Work location: remote
