Clinical Research Assistant

Agbgroupllc; Providence (RI); On-site; USD 40,000 - 80,000; Full time

Job summary

An established clinical research facility is seeking a Clinical Research Assistant to support innovative medical trials in Providence, RI. This entry-level role offers a unique opportunity to contribute to groundbreaking research while ensuring the safety and privacy of participants. You will assist in various clinical tasks, maintain documentation, and communicate effectively with patients and research teams. With a commitment to fostering a supportive work environment, this organization values its employees' professional growth and offers a four-day work week, comprehensive benefits, and a collaborative atmosphere. If you're passionate about making a difference in healthcare, this position is for you.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

401(K) with Employer Match

Paid Time Off

Short Term Disability

Long Term Disability

Life Insurance

Employee Assistance Program

Flexible Spending Accounts

Qualifications

• Prior experience in a clinical environment preferred.
• LPN, RN, or other medical licensure or certification preferred.

Responsibilities

• Support clinical trial performance and maintain documentation.
• Collect initial psychiatric and medical information by interviewing patients.
• Perform clinical tasks including vital signs and specimen packaging.

Skills

Verbal Communication

Written Communication

Interpersonal Skills

Time Management

Organizational Skills

Education

High School Diploma or GED

Bachelor's Degree

Job description

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At K2 Medical Research, a privately-owned clinical research facility in the greater Orlando and Central Florida area, we specialize in conducting multiphasic clinical trials that promote the development of innovative and effective medical treatments while maintaining the safety and privacy of our participants. We are committed to fighting the diseases that plague our loved ones and ourselves. By harnessing the power of advanced clinical research and connecting our patients with the treatments of tomorrow, we can improve the health of our local communities, and by extent, the population of our world.

K2 is seeking a Clinical Research Assistant for our Providence, RI clinic.

The Clinical Research Assistant will:

• Support clinical trial performance and conduct congruent to the philosophy and mission of K2 Medical Research. Promote good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federal regulations and K2 Medical Research guidelines (SOPs) for the enrollment and maintenance of subjects in clinical trials, and by collecting, recording, and maintaining source and sponsor documentation.

Primary Responsibilities:

• Understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator
• Assist the Site Director and Project Management team on projects as needed
• Adhere strictly to the study protocol; obtain exemptions when necessary/appropriate
• Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub-Investigator
• Articulate all pertinent issues to the PI or document by email/letter or during meetings
• Collect initial psychiatric and medical information by interviewing patients and by accessing other appropriate sources
• Ensure a flow of communication including telephone conferences between patient, study staff, referral sources, Sponsor and/or CRO, Monitors, Auditors and any marketing groups hired by the Sponsor
• Utilize various psychiatric rating scales and maintain interrater reliability with other clinicians at Compass Research
• Perform clinical tasks including, but not limited to, vital signs, height and weight, ECG, phlebotomy, specimen packaging
• Maintain timely K2 Medical Research source documentation as well as sponsor required information.
• Dispense and maintain accurate records of study medication
• Educate patients and family regarding their study and clinical drug trials in general.
• Complete all monitor and sponsor queries in a timely manner
• Provide appropriate community resource referrals to patients, caretakers, and family at conclusion of patient's participation in study

Knowledge, Skills, and Abilities:

• Outstanding verbal and written communication skills
• Excellent interpersonal and customer service skills
• Strong time management and organizational skills; in-depth knowledge of industry regulations
• Proven ability to foster mentoring relationships
• Ability to create momentum and foster organizational change

Qualifications:

• HS Diploma or GED transcript required. Bachelor's degree strongly preferred.
• Prior experience in a clinical environment preferred. Experience in clinical research is ideal.
• LPN, RN, or other medical licensure or certification preferred.
• Applicants that don't meet 100% of the above qualifications but have a combination of related education, applicable experience, demonstrated capability, and a genuine passion for success in this position may also be considered.

At K2, we value our employees and their professional and personal needs, and support these through our benefit offerings:

• Medical, Dental, Vision, Flexible Spending Accounts, Employer paid Long-Term disability and Life Insurance, Short Term Disability, Accident and Critical Illness Insurance, Voluntary Life and Long-Term Care Insurance, Legal Shield, Employee Assistance Program, and various discount programs.
• 401(K) Plans- Traditional and Roth plans are available; 4% employer match that is immediately vested
• PTO of 16 days per year, 17 days after the first year of FT employment
• 9 paid Holidays
• K2 observes a four-day work week, Monday through Thursday, for full time employees. Fridays are non-working days unless required by business needs.

Seniority level

• Entry level

Employment type

• Full-time

Job function

• Research, Analyst, and Information Technology

Industries

• Truck Transportation

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