Clinical Research Assistant

Headlands Research; Pikesville (MD); On-site; USD 35,000 - 45,000; Full time

Job summary

A clinical trial organization is seeking a Clinical Research Assistant in Pikesville, MD. This entry-level role involves assisting coordinators in clinical trial operations, performing phlebotomy, and ensuring accurate data entry. Candidates should have strong communication skills and prefer those with a Certified Medical Assistant qualification. This full-time position offers an opportunity to contribute to innovative research initiatives.

Qualifications

• Experience interacting with patients.
• Clinical research experience preferred.
• Knowledge of medical terminology and laboratory skills preferred.

Responsibilities

• Assist clinical research coordinators in the conduct of clinical trials.
• Perform phlebotomy and vital checks.
• Assist in preparation for study visits.
• Enter data into EDC, CTMS.

Skills

Phlebotomy

Communication skills

Attention to detail

Teamwork

Microsoft Office

Education

Certified Medical Assistant preferred

Job description

Join to apply for the Clinical Research Assistant role at Headlands Research

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting‑edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.

The Role

Pharmasite, a Headlands Research site is looking for a Clinical Research Assistant who is an experienced phlebotomist and/or Certified Medical Assistant to assist coordinators in conducting clinical research study visits.

Responsibilities

• Assist clinical research coordinators in the conduct of clinical trials.
• Perform phlebotomy & vital checks (EKGs, etc.)
• Assist in preparation for study visits
• Assist in the collection of clinical data
• Enter data into EDC, CTMS
• Specimen processing
• Assist with ancillary scheduling
• Order study participant meals
• Process study participant stipends

Requirements

• Certified Medical Assistant preferred
• Experience interacting with patients
• Clinical research experience preferred
• Knowledge of medical terminology and laboratory skills preferred
• Knowledge of Microsoft Office required
• Excellent interpersonal and communication skills—interact effectively with patients, staff, sponsors, and others as required.
• High attention to detail
• Ability to set priorities and meet deadlines
• Ability to work as a member of a team

Seniority level

• Entry level

Employment type

• Full‑time

Job function

• Research, Analyst, and Information Technology
• Research Services

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