Clinical Research Associate - Remote

SOLVENTUM; United States; Remote; USD 106,000 - 146,000; Full time

Job summary

Solventum seeks a Clinical Research Associate for remote work to support global studies. You will monitor sites, ensure regulatory compliance, and maintain trial master files. This role requires CRA monitoring experience and strong communication as you collaborate with diverse teams.

Expect up to 75% travel and a commitment to protecting participant data while ensuring study quality. US work authorization is required; relocation is not offered.

Qualifications

• Bachelor’s degree or higher with 3 years of clinical research or medical device experience, including 2 years CRA monitoring.
• OR High School Diploma with 7 years of clinical research experience including 5 years CRA monitoring.
• Experience with hospital/clinical settings or medical laboratories is a plus.

Responsibilities

• Ensure TMF documents and regulatory files at investigative sites are prepared, collected, and maintained.
• Conduct pre-study site visits and assist in site selection and initiation visits.
• Perform site monitoring visits and address data discrepancies or deficiencies with remedial actions.
• Review CRFs and source documents for accuracy and completeness; resolve queries.
• Collaborate with Clinical Project Manager and cross-functional teams and external partners.
• Assist with device preparation, shipment coordination, and accountability records.

Skills

CRA monitoring experience

Remote work experience

Regulatory training

Communication & training

Cross-functional collaboration

Education

Bachelor's degree or higher

High School Diploma/GED alternative

Tools

Smartsheet

Microsoft Copilot

Microsoft 365

Job description

At Solventum, we improve lives by helping healthcare professionals do their best work. Join a team using innovation and insight to make a real impact on the future of healthcare. All roles listed are with Solventum, and we're committed to protecting your personal information-learn more in our Privacy Policy: https://www.solventum.com/en-us/home/legal/website-privacy-statement/applicant-privacy/

Job Description:

Clinical Research Associate - Remote

3M Health Care is now Solventum

At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers' toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.

We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.

The Impact You'll Make in this Role

As a Clinical Research Associate, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:

• Ensuring preparation, collection, and distribution of trial master file (TMF) documents and maintenance of regulatory files at investigative site
• Conducting pre-study site visits, collecting and reviewing site feasibility and operational processes information, and preparing reports; participating in the final selection of investigators and study sites
• Conducting clinical study site initiation visits; advising and training site personnel on Sponsor and regulatory requirements for study conduct
• Conducting site monitoring visits and following-up to identify significant problems and issues and ensuring that all clinical aspects of studies are being carried out in accordance with state and federal regulations, guidelines and policies
• Reviewing on-site files and records, case report forms, and source documents for completeness, accuracy, consistency, and compliance; identifying deficiencies and discrepancies, and providing remedial training and/or initiating corrective action as required
• Reviewing case report form queries and problems, and clarifying and/or obtaining changes to data as appropriate
• Collaborating closely with the Clinical Project Manager, cross functional study teams and all Research partners, internal and external to company
• Assisting with device preparation, shipment coordination and maintaining appropriate accountability records

Your Skills and Expertise
To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:

• Bachelor’s degree or higher (completed and verified prior to start) from an accredited institution AND three (3) years of clinical research, biomedical, or medical device industry experience in a private, public, government or military environment, which must include two (2) years of direct Clinical Research Associate (CRA) experience conducting clinical study monitoring activities.

OR

• High School Diploma/GED (completed and verified prior to start) AND seven (7) years ofclinical research, biomedical, or medical device industry experience in a private, public, government or military environment, which must include five (5) years of direct Clinical Research Associate (CRA) experience conducting clinical study monitoring activities.

Additional qualifications that could help you succeed even further in this role include:

• Direct CRA monitoring experience monitoring medical device clinical studies.
• Experience working in hospital or clinical setting or medical laboratory
• Uses Smartsheet, Microsoft Copilot, and Microsoft 365 applications to manage, track, analyze, and communicate work-related information.
• Background in preparing and delivering verbal, written, and presentation communications regarding project status, issues, and escalations to relevant stakeholders.
• Identifies problems, evaluates potential solutions, and supports resolution of business or project issues.
• Prioritizes, plans, tracks, and evaluates deliverables against established requirements and timelines.
• Manages multiple concurrent tasks and adjusts priorities based on changing business needs and deadlines.

Work location: Remote

Travel: May include up to 75%

Relocation Assistance: Is not authorized

Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).

Supporting Your Well-being

Solventum offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.

Applicable to US Applicants Only:The expected compensation range for this position is $106,000 - $145,750, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate's relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: https://www.solventum.com/en-us/home/our-company/careers/#Total-Rewards

Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.

Please note, Solventum does not expect candidates in this position to perform work in the unincorporated areas of Los Angeles County.

Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.

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