Our Clinical Research team pushes the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.
Establish an effective relationship with our Company and key institutions
Communicate with sites on issues related to regulatory documentation, financial payments, and upcoming studies
Provide exceptional customer service, facilitating decision making between key institutions and our Company
Collaborate with internal stakeholders, including, but not limited to: Clinical Research Associates , Clinical Research Managers , Site Selection CRMs, Clinical Research Directors, Clinical Operations Managers, Research Scientific Directors, CRA Line Managers, Clinical Quality Management.
Participate in country strategy for upcoming programs as needed
Support Therapeutic Area level territory development and targeted site selection based upon portfolio needs; discuss future studies and review portfolio with key institutions
Support site initiation activities and remediation, as appropriate
Ability to identify, assess, and resolve site management issues, specifically as it relates to site initiation activities
Support continuity with master contracts
Knowledge of assigned institution/organization operational structure
Education & Experience
BS/BA degree in a Biological Science or Nursing
Five to six years of clinical research experience preferred; at least 2 years' experience in a particular Therapeutic Area; previous lead CRA experience preferred
Qualifications, Skills, & Experience
Possess the ability to work independently and in a team environment
Possess strong knowledge of local regulatory and compliance requirements
Knowledge of institution/organization operational structure
Excellent time management, project management, organizational, issue identification, problem-solving, and communication (written and verbal) skills
History of strong performance
Expertise and proficiency of core systems, including trial management systems, and tools
Skills and judgment required to be a good steward/decision-maker for the company
Possess an excellent working knowledge of all applicable International Conference on Harmonisation Good Clinical Practice and FDA regulations
We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we "follow the science" that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.
Who we are
We are known as Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.
What we look for
In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth.
NOTICE FOR INTERNAL APPLICANTS
In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.
If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor.
US and Puerto Rico Residents Only:
If you need an accommodation for the application process please email us at email@example.com
For more information about personal rights under Equal Employment Opportunity, visit:
EEOC GINA Supplement
OFCCP EEO Supplement
OFCCP Pay Transparency Rule
We are an equal opportunity employer, Minority/Female/Disability/Veteran - proudly embracing diversity in all of its manifestations.
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
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Merck & Co., Inc.