Nurse/Clinical Research Coordinator Jobs In Spain

Nurse/Clinical Research Coordinator Jobs In Spain

Nurse/Clinical Research Coordinator Jobs In Spain
Nurse/Clinical Research Coordinator Jobs In Spain
Job Title
Registered Nurse/Clinical Research Coordinator
Job ID
27754084
Location
Myrtle Beach, SC, 29572 

Description

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, devoted entirely to oncology clinical research. Throughout its existence, START has given cancer patients hope in global community practices by providing access to cutting-edge studies in the United States and Europe. START’s mission today, with over 1,300 studies completed and research facilities in the United States, Spain, Portugal, and Ireland, is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for cancer patients and eventually lead to a cure. To far, over 43 therapies performed at START sites have received FDA/EMA approval. Interestingly, Academic Medical Centers (AMCs) undertake 80% of cancer trials.

START has the world’s largest roster of Principal Investigators (PIs) across eight clinical trial locations. START is dedicated to quickening the transition from trials to medicines, giving hope to patients, families, and clinicians all over the world. For example, in San Antonio, where START was formed, the first patient ever received Keytruda, the most effective cancer treatment in medical history.

We Are Hiring:

We are looking for a dedicated Registered Nurse/Clinical Research Coordinator to join our Myrtle Beach, SC team. In this role, you will manage multiple clinical trials across various therapeutic areas and phases, ensuring compliance with all relevant regulations, Standard Operating Procedures, and study protocols.

This is a full-time position with flexible hours. Our office is open Monday-Friday.

Essential Responsibilities:

  • Conduct clinical research trials in compliance with GCP guidelines and protocols.
  • Screen potential study subjects, document medical histories, and maintain accurate records.
  • Collect and process lab specimens, manage study drug accountability, and administer medications as directed.
  • Ensure compliance with HIPAA and report all adverse events to maintain trial integrity.
  • Coordinate study-related procedures, data entry, and source documentation.
  • Collaborate with investigators and sponsors to uphold study standards and quality.
  • Maintain a professional attitude and foster effective relationships with staff and study personnel.
Best-in-Class Benefits and Perks

We value our employees’ time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including: 

Comprehensive health coverage includes medical, dental, and vision insurance.

  • Robust retirement planning: 401(k) plan is offered with employer matching
  • Financial Security: Life and disability insurance provide further protection.
  • Flexible financial options: Health savings and flexible spending accounts are offered.
  • Wellbeing and Work-Life Balance: Paid time off, flexible schedules, and remote work options are available.
  • Furthermore, we strive to provide the greatest atmosphere for our employees, allowing them to learn and grow with the firm. We try to create a
  • collaborative, creative environment in which everyone feels comfortable contributing to our processes, choices, planning, and culture.

 More about The START Center for Cancer Research

Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world.

Are you ready to join a team that is redefining the future of cancer treatment?

Join us on our effort to end cancer one clinical study at a time. Your skills and passion can help us provide hope and healing to patients all across the world. Kindly submit your application online.

We are an equal opportunity employer who values and promotes diversity in the workplace. We do not discriminate based on race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected by federal, state, or local law.

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