Oncology CRA-Sponsor side!

LeoForce; Rockville (MD); Hybrid; USD 125,000 - 140,000; Full time

Benefits offered by this job

Remote work options

Flexible schedule

Job summary

LeoForce in Rockville, MD is seeking a Clinical Research Associate (Mid Level) to support oncology trials in a full-time role with remote or hybrid work options. You will collaborate with a team to advance novel cancer therapies and ensure regulatory compliance across sites.

The ideal candidate has 3–5 years of Oncology CRA experience, a life sciences degree, and strong data management and communication skills. This position offers growth opportunities within a biotech startup environment.

Qualifications

• 3–5 years of Oncology experience as a Clinical Research Associate in biotech/pharma.
• Bachelor's degree in life sciences; advanced degree preferred.
• Thorough understanding of FDA regulations and guidelines.
• Strong organizational and communication skills.

Responsibilities

• Oversee design, implementation, and management of clinical trials from start to finish.
• Ensure sites comply with study protocol, FDA regulations, and applicable rules.
• Conduct site visits to monitor progress, data accuracy and issue resolution.
• Collaborate with investigators and staff to safeguard participant safety and rights.
• Prepare and review study documents such as protocols and informed consent forms.
• Coordinate with data management to ensure accurate data collection.
• Contribute to the presentation of trial results to internal teams and regulators.

Skills

Oncology Clinical Research Experience

FDA Regulations Knowledge

Project & Site Coordination

Excellent Communication

Education

Bachelor's degree in life science

Advanced degree preferred

Tools

Clinical Trial Management Systems

Job description

6903352

a day ago

Job Description

Experience: Mid Level

Salary: $125,000 - $140,000 per year

Job Details

We are seeking 1 Clinical Research Associate's (CRA) to join our biotech startup. This is a full-time position that offer the opportunity to work on groundbreaking clinical research projects. The successful candidate will have the chance to collaborate with a team of highly skilled professionals and contribute to the development of innovative medical treatments and therapies.

Responsibilities

1. 1. Assisting with the oversight of the design, implementation, and management of clinical trials from inception to completion.
2. 2. Ensuring the clinical sites are compliant with the study protocol, FDA regulations, and other applicable regulatory requirements.
3. 3. Conducting site visits to assess the progress of the trials, verify data accuracy, and resolve any issues that may arise.
4. 4. Collaborating with investigators and other clinical staff to ensure the safety and rights of the participants are protected.
5. 5. Preparing and reviewing study-related documents such as protocols, informed consent forms, and case report forms.
6. 6. Coordinating with the data management team to ensure the data collected is accurate and reliable.
7. 7. Participating in the preparation and presentation of clinical trial results to internal teams, regulatory agencies, and other stakeholders.

Qualifications

1. 1. A bachelor's degree in a life science, nursing, or a related field. An advanced degree is preferred.
2. 2. A minimum of 3-5 years of Oncology experience as a Clinical Research Associate in the biotech/pharma space.
3. 3. Proven experience in managing/co-managing clinical trials, including experience with different phases of clinical research.
4. 4. A thorough understanding of FDA regulations and guidelines related to clinical research.
5. 5. Strong organizational skills with the ability to manage multiple tasks and meet deadlines.
6. 6. Excellent communication and interpersonal skills, with the ability to interact effectively with a diverse team of professionals.
7. 7. Proficient in using clinical trial management systems and other related software.
8. 8. Experience with solid tumors is a must.

This position offers a unique opportunity to contribute to the advancement of medical science and improve patient outcomes.

A bit about us

We are a small, clinical stage biotech focused on developing novel medicines for cancer. We are hiring 1 CRA on a remote or hybrid basis, with strong experience in Oncology.

Why join us?

• Financially stable, late phase biotech company
• Strong pipeline
• Opportunity for growth
• Flexible Schedule

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