Associate Director, Clinical Research Job

3 days left

Rahway NJ
Oct 14, 2016
Oct 24, 2016
Organization Type
Clinical Practice
Associate Director, Clinical Research-CLI005329


Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The CRM has a significant impact on how a country can deliver country-specific trial commitments and objectives. As a customer-facing role, this position will build business relationships and represent Merck with investigators, functional outsourcing partners and other external partners and therefore have a significant impact on country-level customer relationships.

The position requires the ability to make decisions independently and oversee important activities relevant to clinical research activities in the country according to predetermined global policies and commitments with the support, oversight and supervision of the Country Research Director. Requires strong understanding of local regulatory environment for the individual to weigh pros and cons of key decisions with input from manager.

Primary activities/responsibilities include but are not limited to:

The incumbent is accountable for the performance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Merck policies and procedures, quality standards and adverse event reporting requirements internally and externally.

The CRM is the country point of contact (POC) for assigned protocols and pro-actively drives/tracks execution and performance of deliverables/timelines/results to meet country commitments, requiring strong collaboration with local Country Operations roles.

The CRM is responsible for quality and compliance for assigned protocols in the country and oversees CRAs and/or CTCs and training compliance. Performs quality control visits, reviews Monitoring Visit Reports and escalates performance issues and training needs to functional vendor and internal management as needed.

The CRM is responsible for collaboration and relationship management with investigators for insourced and outsourced studies, with functional outsourcing vendors and other external partners. The CRM oversees country and site validations, site selection and recruitment in assigned protocols.

The CRM is responsible for clinical trial education to sites.

The ability to identify problems, conflicts and opportunities early and lead, analyses and prepare mitigation plans and drive conflict resolution is critical. The position requires skillful negotiation in tough situations with both internal and external groups; settle differences with minimum noise; win concessions without damaging relationships; be direct and forceful as well as diplomatic; gain trust quickly from other parties in negotiations and have an excellent sense of timing.


Education Minimum Requirement:

- Bachelor’s degree or equivalent with 8+ years of experience in Clinical Research, OR a Master’s degree with 6+ years of experience in clinical research, OR a PhD/MD with 3+ years of clinical research experience.

Required Experience and Skills:

- Strong understanding of clinical trial planning, (site) management and metrics.

- Strong communication, diplomatic and empathic skills.

- Strong leadership skills (scientific and business) and proven ability to coordinate and lead local teams to high performance.

- Strong organizational skills with demonstrated success required.

- Excellent oral and written English language skills.

- Problem solving and conflict resolution.

- Negotiation skills with both internal and external groups.

Preferred Experience and Skills:

- Experience with managing clinical trials within a country from site selection to site close out.

- Experience working in a matrix environment.

- Experience in Infectious Disease studies.

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

For more information about personal rights under Equal Employment Opportunity, visit:

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Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.

Job: Clinical Research Monitor

Job Title:Assoc. Dir, Clinical Research

Primary Location: NA-US-NJ-Rahway

Employee Status: Regular

Travel: Yes, 50 % of the Time

Number of Openings: 1

Hazardous Materials: None

Company Trade Name:Merck