Senior Field Clinical Specialist
WFA Digital Insight
As the demand for medical device clinical trial specialists continues to rise, with over 12% growth expected by 2027, professionals with expertise in this area are in high demand. Abbott's commitment to innovation and employee development makes this role particularly attractive, with opportunities for career advancement and professional growth. With the healthcare industry's increasing focus on technology and research, candidates with a strong background in medical affairs and clinical trial management will be well-positioned for success. Before applying, candidates should be aware of the 80% travel requirement and the need for strong communication and project management skills.
Job Description
About the Role
The Senior Field Clinical Specialist plays a critical role in Abbott's Vascular division, overseeing clinical trials and research activities across the Midwest and Central Southern region. This position requires a deep understanding of medical affairs, as well as the ability to execute complex projects and develop innovative solutions. As a key member of the team, the Senior Field Clinical Specialist will work closely with cross-functional teams to drive business results and advance the company's mission.The day-to-day responsibilities of this role will involve directing human clinical trials, phases III & IV, and overseeing data collection activities. The successful candidate will be responsible for recruiting clinical investigators, negotiating study design and costs, and ensuring compliance with regulatory requirements. This role will also involve collaborating with internal stakeholders to develop and implement clinical protocols, as well as providing reporting information to regulatory agencies.
Abbott's commitment to employee development and growth provides a unique opportunity for professionals to advance their careers and gain valuable experience in the medical device industry. With a strong focus on innovation and customer satisfaction, Abbott is an ideal employer for those looking to make a meaningful impact in the healthcare sector.
What You Will Do
- Direct human clinical trials, phases III & IV, for company products under development
- Oversee data collection activities and ensure compliance with regulatory requirements
- Recruit clinical investigators and negotiate study design and costs
- Collaborate with internal stakeholders to develop and implement clinical protocols
- Provide reporting information to regulatory agencies
- Monitor adherence to protocols by clinicians within a clinical setting
- Coordinate and oversee investigator initiations and group studies
- Participate in adverse event reporting and safety responsibilities monitoring
- Act as a consultant/liaison with other corporations when working under licensing agreements
- Develop and maintain relationships with key stakeholders, including clinical investigators and regulatory agencies
- Stay up-to-date with industry trends and developments, applying this knowledge to drive business results
What We Are Looking For
- Associate's Degree in a relevant field
- 7+ years of relevant experience in medical affairs or a related field
- Strong knowledge of clinical trial management and medical device regulations
- Excellent communication and project management skills
- Ability to work independently and as part of a cross-functional team
- Strong analytical and problem-solving skills
- Experience with Excel and other Microsoft Office applications
- Ability to travel up to 80% of the time
Nice to Have
- RN or RT with Cath Lab experience
- Medical device clinical trial and/or research experience
- Experience working in a fast-paced, dynamic environment
- Strong understanding of regulatory requirements and industry trends
Benefits and Perks
- Competitive salary and benefits package
- Opportunity for career advancement and professional growth
- Comprehensive health and wellness benefits
- Retirement savings plan with employer contribution
- Tuition reimbursement and education benefits
- Flexible work arrangements, including remote work options
- Access to cutting-edge technology and innovative products
- Collaborative and dynamic work environment
- Recognition and reward programs for outstanding performance
How to Stand Out
- Develop a strong understanding of clinical trial management and medical device regulations to stand out as a candidate.
- Highlight your experience with Excel and other Microsoft Office applications, as well as any relevant certifications or training.
- Be prepared to discuss your experience working in a fast-paced, dynamic environment and your ability to travel up to 80% of the time.
- Tailor your resume and cover letter to the specific requirements of the role, emphasizing your skills and experience in medical affairs and clinical trial management.
- Research the company culture and values to demonstrate your enthusiasm for the role and the company, and to show that you are a strong fit for the team.
- Prepare examples of your experience working with cross-functional teams and your ability to communicate complex information to non-technical stakeholders.
- Be prepared to negotiate salary and benefits, and do not be afraid to ask questions about the role and the company during the interview process.
This is a remote position listed on WFA Digital, the platform for professionals who work from anywhere. Browse more remote jobs across all categories.