Conventional/Manual Machinist

Ex-MilitaryCareers.com USA; Newark (NJ); On-site; USD 70,000 - 85,000; Full time

Job summary

Join a forward-thinking company as a Clinical Research Coordinator, where you will manage and oversee clinical trials in Gynecologic Oncology. This is a unique opportunity to contribute to groundbreaking research that impacts patient care. You will collaborate with healthcare professionals, ensuring trials adhere to ethical standards and regulations. With a focus on communication and organization, you'll play a vital role in the success of clinical studies. If you're passionate about improving patient outcomes and ready to make a difference, this position is perfect for you.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

401K with Match

Paid Time Off (PTO)

Sick PTO

Qualifications

• 3+ years of experience in clinical research coordination.
• Excellent knowledge of clinical trial design and management.

Responsibilities

• Oversee day-to-day management of clinical trials including patient recruitment.
• Ensure compliance with ethical standards and regulatory requirements.

Skills

Clinical Research Coordination

Fluency in English

Fluency in Spanish

Knowledge of GCP Guidelines

Organizational Skills

Problem-Solving Skills

Communication Skills

Education

Bachelor's Degree in Related Field

Tools

Clinical Trial Management Systems

Job description

Clinical Research Coordinator Temp to Hire

This Jobot Consulting Job is hosted by: Ba Tran
Are you a fit? Easy Apply now by clicking the "Apply" button and sending us your resume.
Salary: $70,000 - $85,000 per year

A bit about us:

We are seeking an experienced Consulting Clinical Research Coordinator to join our healthcare team. This is an exciting opportunity to be part of a team that is at the forefront of clinical research in the healthcare industry. You will play a crucial role in managing and overseeing clinical trials, ensuring they are conducted in accordance with ethical standards and regulations. You will be directly involved in groundbreaking research that has the potential to significantly impact patient care and treatment outcomes in the field of Gynecologic Oncology (GynOnc). This position requires fluency in English and Spanish.

Why join us?

Medical , Dental and Vision Insurance
401K w/ Match
Temp to Hire opportunity
PTO
Sick PTO
and more!

Job Details

ENGLISH/SPANISH FLUENCY REQUIRED

Is your background a match?

• Bachelor's degree in a related field preferred
• 3+ years of experience in clinical research coordination
• English/Spanish fluency REQUIRED
• Prior experience in Gynecologic Oncology (GynOnc) is a plus!
• Excellent knowledge of clinical trial design, management, and regulatory requirements
• Strong understanding of Good Clinical Practice (GCP) guidelines
• Exceptional organizational skills and ability to manage multiple clinical trials simultaneously
• Excellent communication and interpersonal skills
• Proficient in using clinical trial management systems and other related software
• Ability to work effectively in a team and independently
• Detail-oriented with strong problem-solving skills
• Proven ability to maintain confidentiality and handle sensitive information with discretion
• Willingness to stay updated on the latest trends, developments, and advancements in the field of GynOnc
• Commitment to improving patient care and treatment outcomes through clinical research
• NOTE: We are fully onsite (M-F) at our Fountain Valley, CA location; hybrid not available

What will you be doing?

• Oversee the day-to-day management of clinical trials, including but not limited to, patient recruitment, data collection, and data analysis
• Ensure all clinical trials are conducted in accordance with the study protocol, ethical standards, and regulatory requirements
• Coordinate with physicians, nurses, and other healthcare professionals to ensure patient safety and the integrity of clinical trial data
• Develop and maintain effective relationships with study sponsors, investigators, and other key stakeholders
• Prepare and submit regular reports on the progress and results of clinical trials
• Participate in the development of study protocols, informed consent forms, and case report forms
• Identify, evaluate, and manage potential risks and issues related to clinical trials
• Provide training and guidance to other members of the clinical research team
• Stay updated on the latest trends, developments, and advancements in the field of GynOnc

Interested in hearing more? Easy Apply now by clicking the "Apply" button.

Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.

Receive updates & notifications from Ex-MilitaryCareers.com USA