Clinical Evidence Planning and Evaluations Manager

Job Title:

Clinical Evidence Planning and Evaluations Manager Location:

Washington, PA Employment Type:

Contract(7 months)

Industry:

Manufacturing industry.

Compensation:

$74.17 - 81.32 /

Hour Schedule:

40.00 hrs/Week About the

Opportunity:

This is a role well suited for a self-driven professional looking to expand the impact of Medical Affairs work across the organization. As a Clinical Evidence Planning and Evaluations Manager, you will be responsible for creating and driving the Clinical Evidence Strategy for Varian's devices

Why You'll Love Working Here:

Supportive, team-driven culture that values collaboration, transparency, and accountability Opportunity to grow your career with a global workforce solutions leader serving multiple industries People-first environment that encourages employees to bring their authentic selves to work Strong focus on partnership, innovation, and delivering meaningful results for clients and candidates Why This Opportunity is

Exciting:

This role offers the chance to join a company that prioritizes both people and performance-where your contributions directly impact client success while giving you room to grow and develop professionally. About Acara Solutions Acara is a premier recruiting and workforce solutions provider-we help companies compete for talent. With a legacy of experience across industries worldwide, we partner with clients, listen to their needs, and customize visionary talent solutions that drive the business outcomes they seek. We leverage decades of experience to deliver contingent staffing, direct placement, executive search, and workforce services worldwide. Sound like a good fit?

APPLY TODAY

What You'll Do:

Creation of Clinical Evaluation Plans, Reports, and Post-Market Clinical Evaluation Plans, and Reports (CEP/CER and

PMCFP/PMCFR

) Providing clinical perspective and input to cross-functional teams regarding clinical development, risk management, product management, and post-market surveillance Execute Post-Market Clinical Follow Up activities (may include customer surveys, annual literature searches, clinical studies) Provide clinical review of promotional material and claims in support of publishing customer facing content

What You'll Bring:

Master's Degree in Biophysics, Biomedical Engineering. 2+ years of experience with clinical evaluations, medical physics, or related field.

What Sets You Apart:

PhD Degree in Medical Physics or Biophysics or Biomedical Engineering. You have familiarity with design and manufacture medical devices, especially those used in the radiation oncology setting You have exemplary technical writing and verbal communication skills Understanding of Clinical Evaluation and Post Market Clinical Follow Up Requirements of class I-III medical devices as designated in the European Union Medical Device Regulation (EU MDR)

Additional Information:

Upon offer of employment, the individual will be subject to a background check. After you apply, you may receive a call or message from our AI Talent Scout about this role or other opportunities that match your skills and preferences. AI agent role is to help speed up your hiring process by answering questions, confirming basic information, and identifying whether there's a mutual fit. The call or chat may be recorded so that our recruiting team can review it - they make all final hiring decisions, while AI agent simply helps move you forward faster. The best part? They are available 24/7, so you can connect whenever it's convenient for you. Aleron companies (Acara Solutions, Aleron Shared Resources, Broadleaf Results, Lume Strategies, TalentRise, Viaduct) are an Equal Opportunity Employer. Race/Color/Gender/Religion/National Origin/Disability/Veteran. Applicants for this position must be legally authorized to work in the United States. This position does not meet the employment requirements for individuals with

F-1 OPT STEM

work authorization status.