Careers

Responsibilities

Performing study related procedures including but not limited to:

• Consenting patients
• Taking EKG's and vital signs
• Completing all study-related documents in a timely manner
• Ensure Patient Compliance to Protocol
• Ensure that GCP and FDA guidelines are followed
• Work with sponsoring pharmaceutical and/or device company to ensure that all required duties are completed
• Dispense and account for investigational drug and/or devices

Requirements

• Must have excellent communication skills
• Must have work experience as a Clinical Research Coordinator or related work experience
• Must have flexible schedule and able to work occasional after hours shifts
• Must be highly organized with great attention to detail
• Must thrive in a fast-paced environment and be able to multi-task
• Must be highly self-motivated
• Bachelor's Degree in Science, Nursing or relevant work experience in the field
• Phlebotomy/IV skills preferred
• Experience with diabetes or diabetes education preferred

Compensation:

• This is a full time position with benefits. Salary negotiable depending upon experience.
• Job Type: Full-time Required experience: Clinical Research Coordinator or related work experience required
• Required education: Bachelor's Degree
• Job Type: Full-time
• Pay: $53,000 - $80,000 per year

Benefits

• 401(k)
• 401(k) matching
• Dental insurance
• Employee assistance program
• Flexible schedule
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Parental leave
• Professional development assistance
• Referral program
• Tuition reimbursement
• Vision insurance
• Schedule:

10 hour shift

8 hour shift

Monday to Friday

Supplemental Pay:  Bonus pay

Work Location:  On site in Renton, WA

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The Clinical Research Assistant acts as support staff for the Clinical Research Coordinator team.

This Job Is Ideal for Someone Who Is:

• Dependable -- more reliable than spontaneous
• Adaptable/flexible -- enjoys doing work that requires frequent shifts in direction
• Detail-oriented -- would rather focus on the details of work than the bigger picture
• Achievement-oriented -- enjoys taking on challenges, even if they might fail

Responsibilities:

• Assistance with device studies which may include collection of blood or lab specimens for clinical testing and preparing specimens for shipment
• Data entry support which may include entering data onto paper or web-based electronic data capture systems and data query resolution
• Consenting of patients for research studies
• General clerical assistance for study protocols such as filing, photocopying, supply inventory, restocking supplies, answering phones and other clinic duties as dictated by the study protocols.

Qualifications:

• Excellent attention to detail
• Phlebotomy (and IV) training and experience strongly preferred
• Excellent communication skills
• Time management skills and ability to prioritize workload
• Excellent computer literacy and ability to enter database information quickly and accurately
• Able to read and understand English sufficient to perform duties of the position
• Medical terminology and knowledge of medications preferred
• Medical Assistant Certificate or Bachelors of Science degree preferred
  

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S/he ensures Rainier Clinical Research Center meets all of its required patient contract. This position is ideal for a sociable professional seeking a fast paced, challenging career and is interested in health care.

Reports to: Recruitment and Marketing Manager

Responsibilities:

• Recruits participants for clinical research studies
• Interviews prospective candidates explaining side effects, benefits, qualifications and patient stipend for time and travel
• Contact between 20-50 people a day
• Schedule participants for clinical trials
• Prepares screening questionnaires that outline patient eligibility
• Manages the Clinical Trial Management Software
• Meets and goes beyond study contract goals
• Markets and manages clinical trials on social media
• Blogs regularly about our company through company sponsored social media accounts
• Presents healthcare related information at community functions and health fairs. 

Requirements Education & Experience:

• Bachelors or some college
• Proficient in Microsoft Word, Excel, Facebook, Twitter, and InstaGram

Required Skills:

• Excellent communication skills, communication, multitasking, interpersonal and listening skills
• Ability to make quick but well-thought out decisions, and adapt to changing environments and requirements
• Self-motivated and ability to work well independently as well as using a collaborative team approach
• Ability to adhere to established timelines, processes and procedures
• EEO Statement: Rainier Clinical Research Center is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. 

Job Type: Full-time

Your primary duties will involve administering physical exams, reviewing all study participant data (including medical history, lab work, X-rays, ECG’s, adverse events, protocol compliance throughout all phases of the study process). You will also interact with internal operations team and sponsor companies/CROs to address safety and protocol concerns.

Qualifications:

• Our ideal candidate will have excellent interpersonal skills, with the ability to work collaboratively with our clinical research team. Candidates will handle multiple priorities, have excellent organizational skills, and possess the ability to problem solve to a successful outcome.
• To be considered, candidates must meet the following criteria:
• Must be U.S. Board Certified, preferably Internal Medicine, Endocrinology or Family Medicine.
• Must be licensed in the State of Washington or able to obtain a Washington State license.
• Must hold an unencumbered DEA license. 

Benefits:

Rainier Clinical Research Center values our employees’ time and efforts. Our commitment to your success is enhanced by our competitive compensation and an extensive benefits package.

Other Benefits include:

• Monday-Friday regular hours.
• No Electronic Medical Records system.
• No insurance authorization/ verification required to treat trial participants.
• Malpractice insurance provided.
• 401K
• CME and education allowance
• We work to maintain the best possible environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative environment where each person feels encouraged to contribute to their processes, decisions, planning, and culture.

Job Types: Full-time, Part-time

Pay: From $125.00 per hour