Clinical Strategy Director (3 Openings)

Clinical Strategy Director – Contract – Raritan, NJ. - $100.00-$125.00/hr
The end client is unable to sponsor or transfer visas for this position; all parties authorized to work in the US without sponsorship are encouraged to apply.

A Pharmaceutical Company is seeking a Clinical Strategy Director in Raritan, NJ

Role Description

• The Manager, Clinical Strategy role will develop accurate and effective clinical protocols and associated study registration to align with strategic initiatives.
• Lead in the development of clinical protocols and associated documentation with accountability for successful completion within scope of project deliverables; manage the process to obtain, evaluate and incorporating input resolve from cross-functional reviewers’ input for document finalization
• Lead in the identification and evaluation of competitive research programs to understand clinical strategies
• Determine content (e.g., endpoints, eligibility) and timing of EW THV clinical trial postings in public databases, obtaining input from key stakeholders
• Research and evaluate literature and other data sources to compile applicable clinical inputs for the development of clinical study designs/synopses

Skills & Requirements

• Bachelor’s Degree with 8 years of relevant clinical experience; OR Master’s Degree with 6 years of relevant clinical experience; OR PhD with 4 years of relevant clinical experience
• Experience in clinical trial management, monitoring and/or site management Preferred Qualifications
• Experience writing clinical protocols
• Medical Device industry experience
• Experience in cardiology or interventional cardiology therapeutic areas
• Knowledge of FDA and EU MDR regulations Additional Talents & Expectations
• General knowledge of statistics
• Proven successful clinical project management skills
Proven expertise in Microsoft Office Suite, including Word, Excel, and PowerPoint; publication library software (e.g., EndNote
• Advanced editing and proofreading skills
• Strong problem-solving and critical thinking skills
• Excellent written and verbal communication skills including negotiating and relationship management skills
• Ability to read, write, and speak English fluently
• Extensive knowledge of relevant US and EU regulations and guidelines, Good Clinical and other applicable standards
• Extensive knowledge on conducting focused searches on medical literature database (e.g., PubMed, Medline)
• Ability to travel up to 10% of the time to scientific meetings/conferences and/or to our Irvine, CA corporate

Why Hays?

You will be working with a professional recruiter who has intimate knowledge of the industry and market trends. Your Hays recruiter will lead you through a thorough screening process in order to understand your skills, experience, needs, and drivers. You will also get support on resume writing, interview tips, and career planning, so when there’s a position you really want, you’re fully prepared to get it.

Additionally, this position is a contract role where Hays offers you the opportunity to enroll in full medical, dental or vision benefits.

• Medical
• Dental
• Vision
• 401K
• Life Insurance ($20,000 benefit)

Nervous about an upcoming interview? Unsure how to write a new resume?

Visit the Hays Career Advice section to learn top tips to help you stand out from the crowd when job hunting.

Hays is an Equal Opportunity Employer including disability/veteran.

In accordance with applicable federal and state law protecting qualified individuals with known disabilities, Hays U.S. Corporation will attempt to reasonably accommodate those individuals unless doing so would create an undue hardship on the company. Any qualified applicant or consultant with a disability who requires an accommodation in order to perform the essential functions of the job should call or text 813.336.5570

Drug testing may be required; please contact a recruiter for more information.


Job Type
100.00 - 125.00