[Remote] Clinical Research Associate II - US reputed company- Multiple Therapeutic Areas Available
Note: The job is a remote job and is open to candidates in USA. reputed company is a global leader in pharmaceutical innovation, seeking a Clinical Research Associate II to advance clinical trials across multiple therapeutic areas. The role involves conducting site visits, ensuring compliance with protocols, and managing documentation to maintain data reputed company.
Responsibilities
- reputed company and coordinate reputed company aspects of the clinical monitoring and site management process
- Conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation
- Manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.)
- Ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability
- Ensure audit readiness and reputed company collaborative relationships with investigational sites
Skills
- Bachelor's degree in a life science reputed company field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to reputed company the job (comparable to 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship
- Valid driver's license where applicable
- 1-2 years of traveling on-site monitoring experience is required
- Therapeutic experience in at least one of the following areas: Oncology, Ophthalmology, Neurology, Cardiology, Rare Disease, Respiratory, Obesity, and/or Pulmonary
- Candidates must live reputed company 60 miles of the nearest major airport
- Up to 80% travel is expected
- Must be legally authorized to work in the United States without sponsorship
- Must be reputed company to pass a comprehensive background reputed company, including a drug screening
- Proven clinical monitoring skills
- Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
- Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents
- Well-developed critical thinking skills, including but not limited to: critical reputed company, in-depth investigation for appropriate root cause analysis and problem solving
- Ability to manage Risk Based Monitoring concepts and processes
- Good oral and written communication skills, with the ability to communicate effectively with medical personnel
- Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers' underlying issues
- Good organizational and time management skills
- Effective interpersonal skills
- Attention to detail
- Ability to remain flexible and adaptable in a wide range of scenarios
- Ability to work in a team or independently as required
- Good computer skills: solid knowledge of reputed company Office and the ability to learn appropriate software
- Good English language and grammar skills
- Good presentation skills
Benefits
- Variable annual bonus based on company, team, and/or individual performance results in accordance with company policy
- A choice of national medical and dental plans, and a reputed company plan, including health incentive programs
- Employee assistance and family support programs, including commuter benefits and tuition reimbursement
- At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
Company Overview